VITROS Chemistry Products Cl-Slides, VITROS Chemistry Products ECO2 Slides, VITROS Chemistry Products GLU Slides

K182072 · Ortho-Clinical Diagnostics, Inc. · CGZ · Oct 30, 2018 · Clinical Chemistry

Device Facts

Record IDK182072
Device NameVITROS Chemistry Products Cl-Slides, VITROS Chemistry Products ECO2 Slides, VITROS Chemistry Products GLU Slides
ApplicantOrtho-Clinical Diagnostics, Inc.
Product CodeCGZ · Clinical Chemistry
Decision DateOct 30, 2018
DecisionSESE
Submission TypeTraditional
Regulation21 CFR 862.1170
Device ClassClass 2

Intended Use

VITROS Chemistry Products Cl- Slides: Rx Only. For in vitro diagnostic use only. VITROS Chemistry Products Cl- Slides quantitatively measure chloride (Cl-) concentration in serum, plasma and urine using VITROS 250/350/5,1 FS and 4600 Chemistry Systems and the VITROS 5600/ XT 7600 Integrated Systems. Chloride measurements are used in the diagnosis and treatment of electrolyte and metabolic disorders such as cystic fibrosis and diabetic acidosis. VITROS Chemistry Products ECO2 Slides: Rx Only. For in vitro diagnostic use only. VITROS Chemistry Products ECO2 Slides quantitatively measure total carbon dioxide (CO2) concentration in serum and plasma using VITROS 250/350/950/5,1 FS and 4600 Chemistry Systems and the VITROS 5600/ XT 7600 Integrated Systems. Bicarbonate/ carbon dioxide measurements are used in the diagnosis and treatment of numerous potentially serious disorders associated with changes in body acid-base balance. VITROS Chemistry Products GLU Slides: Rx Only. For in vitro diagnostic use only. VITROS Chemistry Products GLU Slides quantitatively measure glucose (GLU) concentration in serum, plasma, urine, and cerebrospinal fluid using VITROS 250/350/5,1 FS and 4600 Chemistry Systems and the VITROS 5600/ XT 7600 Integrated Systems. Glucose measurements are used in the diagnosis and treatment of carbohydrate metabolism disorders including diabetes mellitus, neonatal hypoglycemia, and idiopathic hypoglycemia, and of pancreatic islet cell carcinoma.

Device Story

VITROS Chemistry Products (Cl-, ECO2, GLU) are multilayered analytical slides for use on VITROS Integrated Systems. Cl- slides use direct potentiometry (ion-selective electrode) to measure chloride ions; ECO2 slides use enzymatic endpoint reactions (phosphoenolpyruvate carboxylase/malate dehydrogenase) to measure total CO2 via NADH absorbance; GLU slides use colorimetric enzymatic reactions (glucose oxidase/peroxidase) to measure glucose. Samples (serum, plasma, urine, CSF) are deposited on slides; spreading layers distribute sample; chemical reactions produce measurable signals (electrical potential, absorbance, or reflected light). Systems are used in clinical laboratories by trained personnel. Output provides quantitative analyte concentrations to clinicians for diagnosis and treatment monitoring of metabolic and electrolyte disorders. Benefits include rapid, automated, high-throughput diagnostic testing.

Clinical Evidence

Bench testing only. Precision/reproducibility evaluated per CLSI EP05-A3 (n=80 per analyte). Linearity evaluated per CLSI EP06-A. Detection limits (LoB, LoD, LoQ) evaluated per CLSI EP17-A2. Interference testing performed per CLSI EP07-A2. Method comparison study (n=125 per analyte) demonstrated high correlation (r=1.00) between VITROS XT 7600 and predicate VITROS 5600 systems.

Technological Characteristics

Thin-film MicroSlide format. Cl-: Potentiometric (ISE). ECO2: Enzymatic endpoint (phosphoenolpyruvate carboxylase/malate dehydrogenase). GLU: Colorimetric (glucose oxidase/peroxidase). Instrumentation: VITROS XT 7600 Integrated System. Connectivity: Integrated system. Software: Automated sample quality index (MicroSensor) for HIT indices.

Indications for Use

Indicated for quantitative measurement of chloride, total carbon dioxide, and glucose in human serum, plasma, urine, and/or cerebrospinal fluid to aid in diagnosis/treatment of electrolyte, metabolic, acid-base, and carbohydrate disorders (e.g., diabetes, cystic fibrosis). Rx only.

Regulatory Classification

Identification

A chloride test system is a device intended to measure the level of chloride in plasma, serum, sweat, and urine. Chloride measurements are used in the diagnosis and treatment of electrolyte and metabolic disorders such as cystic fibrosis and diabetic acidosis.

Predicate Devices

Related Devices

Submission Summary (Full Text)

{0}------------------------------------------------ Image /page/0/Picture/0 description: The image contains the logo of the U.S. Food and Drug Administration (FDA). On the left is the Department of Health & Human Services logo. To the right of that is the FDA logo, which is a blue square with the letters "FDA" in white. To the right of the blue square is the text "U.S. FOOD & DRUG ADMINISTRATION" in blue. October 30, 2018 Ortho-Clinical Diagnostics, Inc. Marlene Hanna Director, Regulatory Affairs 100 Indigo Creek Drive Rochester, NY 14626 Re: K182072 Trade/Device Name: VITROS Chemistry Products Cl-Slides VITROS Chemistry Products ECO2 Slides VITROS Chemistry Products GLU Slides Regulation Number: 21 CFR 862.1170 Regulation Name: Chloride test system Regulatory Class: Class II Product Code: CGZ, KHS, CGA Dated: July 30, 2018 Received: August 1, 2018 Dear Marlene Hanna: We have reviewed your Section 510(k) premarket notification of intent to market the device referenced above and have determined the device is substantially equivalent (for the indications for use stated in the enclosure) to legally marketed predicate devices marketed in interstate commerce prior to May 28, 1976. the enactment date of the Medical Device Amendments, or to devices that have been reclassified in accordance with the provisions of the Federal Food, Drug, and Cosmetic Act (Act) that do not require approval of a premarket approval application (PMA). You may, therefore, market the device, subject to the general controls provisions of the Act. Although this letter refers to your product as a device, please be aware that some cleared products may instead be combination products. The 510(k) Premarket Notification Database located at https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm identifies combination product submissions. The general controls provisions of the Act include requirements for annual registration, listing of devices, good manufacturing practice, labeling, and prohibitions against misbranding and adulteration. Please note: CDRH does not evaluate information related to contract liability warranties. We remind you, however, that device labeling must be truthful and not misleading. If your device is classified (see above) into either class II (Special Controls) or class III (PMA), it may be subject to additional controls. Existing major regulations affecting your device can be found in the Code of Federal Regulations, Title 21, Parts 800 to 898. In addition, FDA may publish further announcements concerning your device in the Federal Register. {1}------------------------------------------------ Please be advised that FDA's issuance of a substantial equivalence determination does not mean that FDA has made a determination that your device complies with other requirements of the Act or any Federal statutes and regulations administered by other Federal agencies. You must comply with all the Act's requirements, including, but not limited to: registration and listing (21 CFR Part 807); labeling (21 CFR Part 801 and Part 809); medical device reporting of medical device-related adverse events) (21 CFR 803) for devices or postmarketing safety reporting (21 CFR 4, Subpart B) for combination products (see https://www.fda.gov/CombinationProducts/GuidanceRegulatoryInformation/ucm597488.html; good manufacturing practice requirements as set forth in the quality systems (QS) regulation (21 CFR Part 820) for devices or current good manufacturing practices (21 CFR 4, Subpart A) for combination products; and, if applicable, the electronic product radiation control provisions (Sections 531-542 of the Act); 21 CFR 1000-1050. Also, please note the regulation entitled, "Misbranding by reference to premarket notification" (21 CFR Part 807.97). For questions regarding the reporting of adverse events under the MDR regulation (21 CFR Part 803), please go to http://www.fda.gov/MedicalDevices/Safety/ReportaProblem/default.htm. For comprehensive regulatory information about mediation-emitting products, including information about labeling regulations, please see Device Advice (https://www.fda.gov/MedicalDevices/DeviceRegulationandGuidance/) and CDRH Learn (http://www.fda.gov/Training/CDRHLearn). Additionally, you may contact the Division of Industry and Consumer Education (DICE) to ask a question about a specific regulatory topic. See the DICE website (http://www.fda.gov/DICE) for more information or contact DICE by email (DICE@fda.hhs.gov) or phone (1-800-638-2041 or 301-796-7100). Sincerely, Kellie B. Kelm -S for Courtney H. Lias, Ph.D. Director Division of Chemistry and Toxicology Devices Office of In Vitro Diagnostics and Radiological Health Center for Devices and Radiological Health Enclosure {2}------------------------------------------------ # Indications for Use 510(k) Number (if known) k182072 Device Name VITROS Chemistry Products Cl- Slides VITROS Chemistry Products ECO2 Slides VITROS Chemistry Products GLU Slides Indications for Use (Describe) 1. VITROS Chemistry Products CI- Slides: Rx Only. For in vitro diagnostic use only. VITROS Chemistry Products Cl-Slides quantitatively measure chloride (Cl-) concentration in serum, plasma and urine using VITROS 250/350/5,1 FS and 4600 Chemistry Systems and the VITROS 5600/ XT 7600 Integrated Systems. Chloride measurements are used in the diagnosis and treatment of electrolyte and metabolic disorders such as cystic fibrosis and diabetic acidosis. 2. VITROS Chemistry Products ECO2 Slides: Rx Only. For in vitro diagnostic use only. VITROS Chemistry Products ECO2 Slides quantitatively measure total carbon dioxide (CO2) concentration in serum and plasma using VITROS 250/350/950/5,1 FS and 4600 Chemistry Systems and the VITROS 5600/ XT 7600 Integrated Systems. Bicarbonate/ carbon dioxide measurements are used in the diagnosis and treatment of numerous potentially serious disorders associated with changes in body acid-base balance. 3. VITROS Chemistry Products GLU Slides: Rx Only. For in vitro diagnostic use only. VITROS Chemistry Products GLU Slides quantitatively measure glucose (GLU) concentration in serum, plasma, urine, and cerebrospinal fluid using VITROS 250/350/5,1 FS and 4600 Chemistry Systems and the VITROS 5600/ XT 7600 Integrated Systems. Glucose measurements are used in the diagnosis and treatment of carbohydrate metabolism disorders including diabetes mellitus, neonatal hypoglycemia, and idiopathic hypoglycemia, and of pancreatic islet cell carcinoma. Type of Use (Select one or both, as applicable) | | Prescription Use (Part 21 CFR 801 Subpart D) | |--|----------------------------------------------| | | Over-The-Counter Use (21 CFR 801 Subpart C) | #### CONTINUE ON A SEPARATE PAGE IF NEEDED. This section applies only to requirements of the Paperwork Reduction Act of 1995. #### *DO NOT SEND YOUR COMPLETED FORM TO THE PRA STAFF EMAIL ADDRESS BELOW.* The burden time for this collection of information is estimated to average 79 hours per response, including the time to review instructions, search existing data sources, gather and maintain the data needed and complete and review the collection of information. Send comments regarding this burden estimate or any other aspect of this information collection, including suggestions for reducing this burden, to: > Department of Health and Human Services Food and Drug Administration Office of Chief Information Officer Paperwork Reduction Act (PRA) Staff PRAStaff(@fda.hhs.gov "An agency may not conduct or sponsor, and a person is not required to respond to, a collection of information unless it displays a currently valid OMB number." {3}------------------------------------------------ #### 5 510(k) Summary Information This summary of 510(k) safety and effectiveness information is being submitted in accordance with the requirements of SMDA 1990 and 21 CFR 807.92. The assigned 510(k) number is: k182072 #### Submitter's Information Ortho-Clinical Diagnostics, Inc. 100 Indigo Creek Drive Rochester, New York 14626-5101 Phone: (585) 453-4041 Fax: (585) 453-3368 #### Contact Person: Marlene Hanna, RAC Director, Regulatory Affairs #### Date of Preparation: July 30, 2018 #### Device Proprietary Name(s): VITROS Chemistry Products Cl- Slides VITROS Chemistry Products ECO2 Slides VITROS Chemistry Products GLU Slides #### Common Names: Chloride assay Carbon dioxide assay Glucose assay ## Classification Names | VITROS | Product<br>Code | Class | Regulation Section | Panel | |--------|-----------------|----------|---------------------------------------------|-----------| | Cl- | CGZ | Class II | 21 CFR 862. 1170 chloride test system | | | ECO2 | KHS | Class II | 21 CFR 862. 1160 carbon dioxide test system | Clinical | | GLU | CGA | Class II | 21 CFR 862. 1345 glucose test system | Chemistry | {4}------------------------------------------------ ## Predicate Device(s) | No. | New Devices | Predicate Devices | Predicate Device<br>FDA 510(k)<br>Number | |-----|------------------------------------------|------------------------------------------|------------------------------------------| | 1 | VITROS Chemistry<br>Products Cl- Slides | VITROS Chemistry<br>Products Cl- Slides | k162020 | | 2 | VITROS Chemistry<br>Products ECO2 Slides | VITROS Chemistry<br>Products ECO2 Slides | k120765 | | 3 | VITROS Chemistry<br>Products GLU Slides | VITROS Chemistry<br>Products GLU Slides | k163433 | #### Intended Use Statement(s) ## 1. VITROS Chemistry Products Cl- Slides Rx Only. For in vitro diagnostic use only. VITROS Chemistry Products Cl- Slides quantitatively measure chloride (Cl-) concentration in serum, plasma and urine using VITROS 250/350/5,1 FS and 4600 Chemistry Systems and the VITROS 5600/ XT 7600 Integrated Systems. Chloride measurements are used in the diagnosis and treatment of electrolyte and metabolic disorders such as cystic fibrosis and diabetic acidosis. ## 2. VITROS Chemistry Products ECO2 Slides Rx Only. For in vitro diagnostic use only. VITROS Chemistry Products ECO2 Slides quantitatively measure total carbon dioxide (CO2) concentration in serum and plasma using VITROS 250/350/950/5.1 FS and 4600 Chemistry Systems and the VITROS 5600/ XT 7600 Integrated Systems. Bicarbonate/carbon dioxide measurements are used in the diagnosis and treatment of numerous potentially serious disorders associated with changes in body acid-base balance. ## 3. VITROS Chemistry Products GLU Slides ## Rx Only. For in vitro diagnostic use only. VITROS Chemistry Products GLU Slides quantitatively measure glucose (GLU) concentration in serum, plasma, urine, and cerebrospinal fluid using VITROS 250/350/950/5,1 FS and 4600 Chemistry Systems and the VITROS 5600/ XT 7600 Integrated Systems. Glucose measurements are used in the diagnosis and treatment of carbohydrate metabolism disorders including diabetes mellitus, neonatal hypoglycemia, and idiopathic hypoglycemia, and of pancreatic islet cell carcinoma. ## Device Description The VITROS Chemistry MicroSlide range of products (in this case VITROS Chemistry Products Cl- Slides, VITROS Chemistry Products ECO2 Slides, and VITROS Chemistry Products GLU {5}------------------------------------------------ Slides), are combined with the VITROS XT 7600 Integrated System to perform the VITROS CI-, ECO2, and GLU assays. ## Comparison to Predicate Devices The following tables show similarities and differences between the new and predicate devices. | Similarities | | | |------------------------------------|--------------------------------------------------------------------------------------------------------------------------------------------------------------------------------|--------------------------------------------------------------------------------------------------------------------| | Device<br>Characteristic | Candidate<br>VITROS Cl- Slides | Predicate Device<br>VITROS Cl- Slides<br>k162020 | | Intended Use | Rx Only. For in vitro diagnostic<br>use only. VITROS Chemistry<br>Products Cl- Slides quantitatively<br>measure chloride (Cl-)<br>concentration in serum, plasma and<br>urine. | Same | | Method<br>Principle | Potentiometric; Electrode (ISE),<br>Direct (undiluted) | Same | | Reactive<br>Ingredients<br>per cm2 | Silver 0.4 mg and silver chloride<br>0.2 mg | Same | | Sample type | Serum and plasma, urine | Same | | Sample volume | 10 µL | Same | | Measuring<br>Range | Serum: 50.0 -175.0 mmo/L<br>Urine: 15-300 mmol/L | Same | | Differences | | | | Device<br>Characteristic | Candidate<br>VITROS Cl- Slides | Predicate Device<br>VITROS Cl- Slides<br>k162020 | | Instrumentation | VITROS 250/350/950/5,1 FS and<br>4600 Chemistry Systems and the<br>VITROS 5600/ XT 7600 Integrated<br>System | VITROS<br>250/350/950/5,1 FS and<br>4600 Chemistry<br>Systems and the<br>VITROS 5600/<br>XT 7600 Integrated System | VITROS Chemistry Products Cl- Slides Table 1 {6}------------------------------------------------ | Similarities | | | |------------------------------------|---------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------|-----------------------------------------------------------------------------------------------------------| | Device<br>Characteristic | Candidate<br>VITROS ECO2 Slides | Predicate Device<br>VITROS ECO2 Slides<br>K120765 | | Intended Use | Rx Only. For in vitro diagnostic<br>use only. VITROS Chemistry<br>Products ECO2 Slides<br>quantitatively measure total carbon<br>dioxide (CO2) concentration in<br>serum and plasma. | Same | | Basic principle | Enzymatic Endpoint | Same | | Reactive<br>Ingredients<br>per cm2 | Phosphoenolpyruvate carboxylase<br>(bacteria) 0.20 U; malate<br>dehydrogenase (porcine heart) 0.26<br>U; phosphoenolpyruvate<br>0.39 mg and nicotinamide adenine<br>dinucleotide, reduced 0.44 mg | Same | | Wavelength | 340 nm | Same | | Sample type | Serum, plasma | Same | | Sample volume | 6 µL | Same | | Measuring<br>Range | 5-40 mmol/L | Same | | Differences | | | | Device<br>Characteristic | Candidate<br>VITROS ECO2 Slides | Predicate Device<br>VITROS ECO2 Slides<br>k120765 | | Instrumentation | VITROS 250/350/950/5,1 FS and<br>4600 Chemistry Systems and the<br>VITROS 5600/ XT 7600 Integrated<br>System | VITROS<br>250/350/950/5,1 FS and<br>4600 Chemistry<br>Systems and the<br>VITROS 5600<br>Integrated System | Table 2 VITROS Chemistry Products ECO2 Slides {7}------------------------------------------------ | Similarities | | | |-------------------------------------------------------|---------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------|-----------------------------------------------------------------------------------------------------------| | Device<br>Characteristic | Candidate<br>VITROS GLU Slides | Predicate Device<br>VITROS GLU<br>Slides<br>(k163433) | | Intended Use | Rx Only. For in vitro diagnostic use<br>only. VITROS Chemistry Products<br>GLU Slides quantitatively measure<br>glucose (GLU) concentration in<br>serum, plasma, urine, and<br>cerebrospinal fluid | Same | | Basic principle<br>Reactive<br>Ingredients<br>per cm² | Colorimetric | Same | | | Glucose oxidase ( <i>Aspergillus sp.</i> ) 0.77 U;<br>peroxidase (horseradish root) 3.6 U;<br>1,7-dihydroxynaphthalene (dye<br>precursor) 67 µg and 4-<br>aminoantipyrine hydrochloride (dye<br>precursor) 0.11 mg. | Same | | Wavelength | 540 nm | Same | | Sample type | Serum, plasma, urine, CSF | Same | | Sample volume | 6 µL | Same | | Measuring<br>Range | Serum: 20.0-625.0 mg/dL<br>Urine and CSF: 20.0-650.0 mg/dL | Same | | Differences | | | | Device<br>Characteristic | Candidate<br>VITROS GLU Slides | Predicate Device<br>VITROS GLU<br>Slides<br>(k163433) | | Instrumentation | VITROS 250/350/950/5,1 FS and<br>4600 Chemistry Systems and the<br>VITROS 5600/ XT 7600 Integrated<br>System | VITROS<br>250/350/950/5,1 FS<br>and 4600 Chemistry<br>Systems and the<br>VITROS 5600<br>Integrated System | #### VITROS Chemistry Products GLU Slides Table 3 {8}------------------------------------------------ #### Method Comparison Method comparison studies were conducted by testing a minimum of 125 human serum samples with analyte concentrations within the measuring ranges (MR) of chloride, carbon dioxide and glucose assays on the VITROS XT 7600 Integrated System and the VITROS 5600 Integrated System (predicate device). In addition, 125human urine samples were tested for chloride and 125 human urine samples and 125 human CSF samples were tested for glucose on the candidate and predicate test systems. The results are summarized below: | VITROS<br>assay | #<br>Sample<br>S<br>Tested | # Samples<br>< MR,<br>>MR | N | Regression<br>Analysis | Slope | Intercept | Test<br>range | Claimed<br>Measuring<br>Range | |--------------------------|----------------------------|---------------------------|-----|------------------------|-------|-----------|---------------|-------------------------------| | CL-<br>Serum<br>(mmol/L) | 125 | 0 | 125 | Passing<br>Bablok | 1.00 | -0.11 | 51.2-167.5 | 50.0-175.0 | | CI-<br>Urine<br>(mmol/L) | 125 | 2 | 123 | Weighted<br>Deming | 1.00 | -0.11 | 15-290 | 15-300 | | ECO2<br>Serum<br>(mg/dL) | 125 | 1 | 124 | Deming | 0.99 | 0.19 | 7.1-38.4 | 5.0-40.0 | | GLU<br>serum<br>(mg/dL) | 125 | 1 | 124 | Weighted<br>Deming | 1.00 | 0.49 | 22.1-593.8 | 20.0-625.0 | | GLU<br>Urine<br>(mg/dL) | 125 | 0 | 125 | Weighted<br>Deming | 1.00 | 0.28 | 25.3-600.4 | 20.0-650.0 | | GLU<br>csf<br>(mg/dL) | 125 | 0 | 125 | Weighted<br>Deming | 1.00 | 0.22 | 22.9-649.5 | 20.0-650.0 | #### Summary of VITROS XT 7600 Method Comparison Regression Analysis Data MR=measuring range In addition to the above mentioned method comparison studies, testing was performed to determine the precision, linearity, limit of detection, and Interfering substances of the representative VITROS assays on the VITROS XT 7600 System. #### Precision Precision studies were conducted following EP05-A3, Evaluation of Quantitative Measurement Procedures, Approved Guidelines – Third Edition (2014). The study was performed by testing a minimum of two Quality control fluids and three human based precision fluids using the chloride (Cl-), carbon dioxide (ECO2), and glucose (GLU) assays. {9}------------------------------------------------ Samples were analyzed using one VITROS XT 7600 Integrated System over 20 days, with 2 runs per day and 2 replicates per specimen (n=80). | System | Fluid ID | Mean | N | SD | %CV | SD | %CV | SD | %CV | SD | %CV | SD | %CV | |----------------------------|------------|------|----|-----|-----|------------|-----|-------------|-----|-------------|-----|--------------------|-----| | Repeatability (Within Run) | | | | | | Within Day | | Between Day | | Between Cal | | Within Lab (Total) | | | 7600 | CLS-5903-1 | 86 | 80 | 0.4 | 0.5 | 0.5 | 0.6 | 0.6 | 0.7 | 0.6 | 0.7 | 1.0 | 1.2 | | 7600 | CLS-5905-2 | 108 | 80 | 0.4 | 0.4 | 0.6 | 0.5 | 0.7 | 0.7 | 0.7 | 0.6 | 1.2 | 1.1 | | 7600 | CLS-PP1 | 66 | 80 | 0.3 | 0.4 | 0.4 | 0.5 | 0.2 | 0.3 | 0.5 | 0.7 | 0.6 | 0.9 | | 7600 | CLS-PP4 | 127 | 80 | 0.4 | 0.4 | 0.6 | 0.4 | 0.4 | 0.3 | 1.2 | 0.9 | 1.4 | 1.1 | | 7600 | CLS-PP5 | 160 | 80 | 0.6 | 0.4 | 0.6 | 0.4 | 0.4 | 0.2 | 1.6 | 1.0 | 1.8 | 1.1 | | 7600 | CLS-SRM | 106 | 80 | 0.4 | 0.3 | 0.5 | 0.5 | 0.3 | 0.3 | 1.0 | 0.9 | 1.2 | 1.1 | ## Cl- Serum (mmol/L) Precision Table ## Cl- Urine (mmol/L) Precision Table | System | Fluid ID | Mean | N | SD | %CV | SD | %CV | SD | %CV | SD | %CV | SD | %CV | |--------|-------------|------|----|-------------------------------|-----|---------------|-----|----------------|-----|----------------|-----|-----------------------|-----| | | | | | Repeatability<br>(Within Run) | | Within<br>Day | | Between<br>Day | | Between<br>Cal | | Within Lab<br>(Total) | | | 7600 | CLU-66791-1 | 101 | 80 | 0.4 | 0.3 | 0.6 | 0.6 | 0.2 | 0.2 | 0.7 | 0.7 | 0.9 | 0.9 | | 7600 | CLU-66792-2 | 189 | 80 | 0.5 | 0.3 | 0.9 | 0.5 | 0.4 | 0.2 | 2.1 | 1.1 | 2.3 | 1.2 | | 7600 | CLU-PP1 | 22 | 80 | 0.3 | 1.3 | 0.5 | 2.2 | 0.2 | 1.0 | 0.2 | 0.9 | 0.6 | 2.6 | | 7600 | CLU-PP3 | 151 | 80 | 0.4 | 0.3 | 0.5 | 0.4 | 0.5 | 0.3 | 0.6 | 0.4 | 0.9 | 0.6 | | 7600 | CLU-PP5 | 249 | 80 | 0.7 | 0.3 | 1.0 | 0.4 | 1.2 | 0.5 | 3.6 | 1.4 | 3.9 | 1.6 | | 7600 | CLU-URN | 67 | 80 | 0.3 | 0.4 | 0.3 | 0.5 | 0.2 | 0.4 | 0.5 | 0.7 | 0.6 | 0.9 | ## ECO2 (mmol/L) Precision Table | System | Fluid ID | Mean | N | SD | %CV | SD | %CV | SD | %CV | SD | %CV | SD | %CV | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | |----------------------------|-------------|------|----|-----|------|-----|-----|-----|-----|-----|-----|-----|-----|------------|--|--|--|--|--|--|--|--|--|--|--|--|--|-------------|--|--|--|--|--|--|--|--|--|--|--|--|--|-------------|--|--|--|--|--|--|--|--|--|--|--|--|--|--------------------|--|--|--|--|--|--|--|--|--|--|--|--|--| | Repeatability (Within Run) | | | | | | | | | | | | | | Within Day | | | | | | | | | | | | | | Between Day | | | | | | | | | | | | | | Between Cal | | | | | | | | | | | | | | Within Lab (Total) | | | | | | | | | | | | | | | 7600 | ECO2-5903-1 | 26 | 80 | 0.3 | 1.0 | 0.4 | 1.4 | 0.5 | 1.9 | 0.0 | 0.0 | 0.6 | 2.4 | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | 7600 | ECO2-5905-2 | 16 | 80 | 0.3 | 21.7 | 0.4 | 2.5 | 0.1 | 0.6 | 0.3 | 1.8 | 0.5 | 3.1 | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | 7600 | ECO2-PP1 | 8 | 80 | 0.3 | 3.2 | 0.4 | 4.5 | 0.1 | 1.5 | 0.4 | 5.6 | 0.6 | 7.4 | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | 7600 | ECO2-PP3 | 17 | 80 | 0.3 | 1.5 | 0.3 | 2.0 | 0.1 | 0.6 | 0.2 | 1.4 | 0.4 | 2.5 | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | 7600 | ECO2-PP5 | 33 | 80 | 0.3 | 0.8 | 0.4 | 1.3 | 0.4 | 1.2 | 0.3 | 0.8 | 0.6 | 1.9 | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | 7600 | ECO2-SRM | 26 | 80 | 0.2 | 0.8 | 1.1 | 4.2 | 0.4 | 1.5 | 0.0 | 0.0 | 1.2 | 4.4 | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | | {10}------------------------------------------------ # GLU (mg/dL) Serum Precision Table | System | Fluid ID | Mean | N | SD | %CV | SD | %CV | SD | %CV | SD | %CV | SD | %CV | |----------------------------|---------------|------|----|-----|-----|-----|-----|-----|-----|-----|-----|-----|-----| | Repeatability (Within Run) | | | | | | | | | | | | | | | Within Day | | | | | | | | | | | | | | | Between Day | | | | | | | | | | | | | | | Between Cal | | | | | | | | | | | | | | | Within Lab (Total) | | | | | | | | | | | | | | | 7600 | GLUS32-5903-1 | 89 | 80 | 0.4 | 0.4 | 0.6 | 0.7 | 0.5 | 0.6 | 0.0 | 0.0 | 0.8 | 0.9 | | 7600 | GLUS32-5905-2 | 282 | 80 | 1.1 | 0.4 | 1.4 | 0.5 | 1.9 | 0.7 | 1.0 | 0.4 | 2.6 | 0.9 | | 7600 | GLUS32-PP1 | 27 | 80 | 0.2 | 0.7 | 0.3 | 1.2 | 0.3 | 1.1 | 0.2 | 0.9 | 0.5 | 1.8 | | 7600 | GLUS32-PP3 | 116 | 80 | 0.5 | 0.4 | 0.6 | 0.5 | 0.5 | 0.4 | 0.2 | 0.2 | 0.8 | 0.7 | | 7600 | GLUS32-PP5 | 566 | 80 | 1.7 | 0.3 | 2.5 | 0.4 | 2.4 | 0.4 | 5.0 | 0.9 | 6.1 | 1.1 | | 7600 | GLUS32-SRM | 99 | 80 | 0.3 | 0.3 | 0.5 | 0.5 | 0.5 | 0.5 | 0.3 | 0.3 | 0.8 | 0.8 | ## GLU (mg/dL) Urine Precision Table | System | Fluid ID | Mean | N | Repeatability<br>(Within Run) | | Within<br>Day | | Between<br>Day | | Between<br>Cal | | Within Lab<br>(Total) | | |--------|---------------|------|----|-------------------------------|-----|---------------|-----|----------------|-----|----------------|-----|-----------------------|-----| | | | | | SD | %CV | SD | %CV | SD | %CV | SD | %CV | SD | %CV | | 7600 | GLU32-66791-1 | 29 | 80 | 0.2 | 0.6 | 0.4 | 1.3 | 0.3 | 1.2 | 0.4 | 1.4 | 0.7 | 2.2 | | 7600 | GLU32-66792-2 | 285 | 80 | 1.4 | 0.5 | 2.3 | 0.8 | 0.9 | 0.3 | 0.8 | 0.3 | 2.6 | 0.9 | | 7600 | GLU32-PP2 | 102 | 80 | 0.4 | 0.4 | 0.7 | 0.7 | 0.6 | 0.6 | 1.2 | 1.2 | 1.5 | 1.5 | | 7600 | GLU32-PP3 | 232 | 80 | 1.1 | 0.5 | 2.4 | 1.0 | 3.5 | 1.5 | 0.9 | 0.4 | 4.3 | 1.9 | | 7600 | GLU32-PP5 | 593 | 80 | 1.9 | 0.3 | 2.7 | 0.5 | 6.5 | 1.1 | 7.2 | 1.2 | 10.0 | 1.7 | ## GLU (mg/dL) CSF Precision Table | GLU (mg/dL) CSF Precision Table | | | | | | | | | | | | | | |---------------------------------|---------------|------|-------------------------------|-----|------------|-----|----------------|-----|----------------|-----|-----------------------|-----|-----| | | | | Repeatability<br>(Within Run) | | Within Day | | Between<br>Day | | Between<br>Cal | | Within Lab<br>(Total) | | | | System | Fluid ID | Mean | N | SD | %CV | SD | %CV | SD | %CV | SD | %CV | SD | %CV | | 7600 | GLUC32-5706-1 | 36 | 80 | 0.2 | 0.6 | 0.3 | 0.9 | 0.4 | 1.0 | 0.2 | 0.5 | 0.5 | 1.4 | | 7600 | GLUC32-5707-2 | 84 | 80 | 0.4 | 0.5 | 0.5 | 0.6 | 0.3 | 0.4 | 0.2 | 0.2 | 0.6 | 0.8 | | 7600 | GLUC32-CSF | 41 | 80 | 0.2 | 0.5 | 0.3 | 0.6 | 0.3 | 0.9 | 0.2 | 0.4 | 0.5 | 1.2 | | 7600 | GLUC32-PP1 | 28 | 80 | 0.1 | 0.5 | 0.3 | 1.1 | 0.3 | 1.2 | 0.3 | 0.9 | 0.5 | 1.9 | | 7600 | GLUC32-PP4 | 289 | 80 | 1.3 | 0.5 | 1.7 | 0.6 | 1.4 | 0.5 | 2.2 | 0.7 | 3.1 | 1.1 | | 7600 | GLUC32-PP5 | 563 | 80 | 2.6 | 0.5 | 3.7 | 0.7 | 3.6 | 0.6 | 2.8 | 0.5 | 5.8 | 1.0 | {11}------------------------------------------------ ## Linearity Linearity studies were performed according to CLSI EP06-A, Evaluation of the Linearity of Quantitative Measurement Procedures: A Statistical Approved Guideline (2003). VITROS CI- Slides, VITROS ECO2 Slides, and VITROS GLU Slides were tested on the VITROS XT 7600 Integrated System. A series of eleven proportionally related admixtures of low and high test fluids were tested to verify linearity; each sample was tested in triplicate, a minimum of two replicates was acceptable for analysis. The linearity studies support the claimed measuring ranges for the VITROS CI-, VITROS ECO2, and VITROS GLU assays. #### Detection Limits Detection capability studies for each analyte were evaluated based upon CLSI EP17-A2, Evaluation of Detection Capability for Clinical Laboratory Measurements Procedures: Approved Guidelines – Second Edition (2012). Limit of blank (LoB) studies were performed by testing 4 blank samples. Samples were tested in replicates of 6 over 3 days, using 3 lots of reagents, 4 samples every day, for a total of 216 observations (72 results per reagent lot). The LoB value for each assay was defined as the highest value achieved using blank samples with the stated probability (i.e. α.= 5%). Since the data for all assays were non-gaussian, a non-parametric approach was applied that estimates the LoB using the calculated rank position corresponding to the 95th percentile of the distribution of blank values observed." Limit of detection (LoD) studies were performed by testing 4 pools of human samples with analyte concentrations close to the expected detection limit for each analyte. Samples were tested in replicates of 6 over 3 days, using 3 lots of reagents, with the 4 human sample pools every day. for a total of 216 observations (72 results per reagent lot). The data were analyzed according to CLSI EP17-A2, using CLSI-approved statistical software Analyse-it version 4.95.4, Method Validation Edition (Analyse-it Software Limited, Leeds UK). The software calculated LoD using a pooled SD from the low level fluid results and the input LoB value for the assay. determined as described above. The LoD value for the highest resultant value achieved among the combinations of reagent lots and human pools evaluated, with the stated probability (i.e. ß= 5%). Limit of Quantitation studies were performed using 4 pools of low level samples with analyte concentrations close to the expected LoQ of the corresponding assay. Samples were tested in replicates of 4 over 3 days, using 3 lots of reagents, 4 samples every day, for a total of 144 observations (48 results per reagent lot). Ortho defines LoQ as the lowest concentration with an imprecision of ≤20% and percent total allowable error < 8% for chloride (serum); imprecision of ≤5 % and percent total allowable error < 10% for chloride (urine), imprecision of ≤20% and percent total allowable error < 30% for carbon dioxide, and imprecision of __20% and total allowable error < 30% for glucose in serum, urine, and CSF. {12}------------------------------------------------ | | Cl- Serum<br>(mmol/L) | Cl- Urine<br>(mmol/L) | ECO2<br>(mmol/L) | GLU (mg/dL) | | | |-------------|-----------------------|-----------------------|------------------|-------------|------------|------------| | | | | | Serum | Urine | CSF | | LoB | 9.2202 | 3.0965 | 1.9944 | 4.5753 | 6.2966 | 4.0745 | | LoD | 9.9798 | 4.0417 | 2.3522 | 5.2670 | 6.7212 | 4.6992 | | LoQ | 49 | 11 | 3.7 | 13 | 20 | 19 | | Claimed LoQ | 50 | 15 | 5.0 | 20 | 20 | 20 | | Assay Range | 50.0-175.0 | 15-300 | 5.0-40.0 | 20.0-625.0 | 20.0-650.0 | 20.0-650.0 | The results of the detection capability studies for each assay are presented in the table below. ## Specificity Interference Testing was performed in accordance with CLSI EP07-A2. Interference Testing in Clinical Chemistry, Approved Guidance-Second Edition. Clinical and Laboratory Standards Institute. November 2005, using VITROS CI , VITROS ECO2 and VITROS GLU assays. Assays were tested on one VITROS XT 7600 Integrated System ('VITROS XT 7600, Test System) and one VITROS 5600 Integrated System (VITROS 5600. Predicate/Control System). Testing on the representative assays included known chemical interferents, common chemical substances identified with potential to interfere based upon risk assessment, as well as several claimed non-interferents. If hemoglobin, bilirubin, and/or intralipid were not previously identified as known interferents for the representative assays, Hemolysis, Icterus and/or Turbidity (HIT) indices, respectively, were evaluated during testing employed "paireddifference" assessment at a minimum of two analyte levels, as specified by CLSI EP07-A2. *VITROS Chemistry Products MicroSensor™: Sub-system of analyzer that performs automated semi-quantitative sample quality index determinations on serum/plasma and cerebrospinal fluid samples. The sample quality index determinations performed are hemolysis, icterus, and turbidity; also referred to as 'HIT indices' or 'sample integrity indices'. Results were evaluated as follows: Known Interferents: The observed bias was compared to predetermined acceptance criteria (the Maximum Allowable Interference (MAI)) per product design input, and the Claimed Bias derived from product claims. - . If the observed bias was within the MAI criteria (either in a positive or negative direction) and/or less than the Claimed Bias, performance was acceptable. - If the observed bias was greater than the Claimed Bias, the bias was compared to the 95% . Confidence Limit (one-sided) per CLSI EP07-A2. If the Claimed Bias fell within the 95% Confidence Limit, performance was acceptable. Potential Interferents and Non-Interfering Substances: The observed bias was compared to the Maximum Allowable Interference (MAI). - If the observed bias was within the MAI criteria (either in a positive or negative . direction), performance was acceptable. {13}------------------------------------------------ - If the observed bias was greater than the MAI the bias was compared to the 95% ● Confidence Limit (two-sided) per CLSI EP07-A2. If the Claimed Bias fell within the 95% Confidence Limit, performance was acceptable. Results demonstrate acceptable bias on the VITROS XT 7600 versus the VITROS 5600 for currently claimed interferents. The following previously untested analyte/interferent level yielded new information for a currently claimed interferent compound as a result of testing: - 110 mmol/L Cl7 4 mg/dL 4-Aminosalicylate on C1 MicroSlides ● One additional interfering substance was identified as a result of testing: - Triglyceride on Cl¯(s) MicroSlides For the interferent indicated, bias profiles on the VITROS XT 7600 demonstrated equivalent magnitudes to those using the VITROS 5600, using the noted substance. The Instructions for Use (IFU) for the VITROS CI assay has been updated to claim the additional interfering substances. #### Conclusion The conclusions drawn from the nonclinical tests (discussed above) demonstrate the VITROS Chemistry Products Cl- Slides, VITROS Chemistry Product CREA Slides, and VITROS Chemistry Product GLU Slides for use on the VITROS XT 7600 Integrated System are as safe, effective, and perform as well as the predicate devices. The information submitted in the premarket notification is complete and supports a substantial equivalence decision.
Innolitics

Panel 1

/
Sort by
Ready

Predicate graph will load when search results are available.

Embedding visualization will load when search results are available.

PDF viewer will load when search results are available.

Loading panels...

Select an item from Submissions

Click any panel, subpart, regulation, product code, or device to see details here.

Section Matches

Results will appear here.

Product Code Matches

Results will appear here.

Special Control Matches

Results will appear here.

Loading collections...