MICROSCAN MICROSTREP PLUS PANEL NEW ANTIMICROBIAL - CEFOTAXIME

K021111 · Dade Microscan, Inc. · LTT · Jun 6, 2002 · Microbiology

Device Facts

• Record ID: K021111
• Device Name: MICROSCAN MICROSTREP PLUS PANEL NEW ANTIMICROBIAL - CEFOTAXIME
• Applicant: Dade Microscan, Inc.
• Product Code: LTT · Microbiology
• Decision Date: Jun 6, 2002
• Decision: SESE
• Submission Type: Traditional
• Regulation: 21 CFR 866.1640
• Device Class: Class 2

Intended Use

To determine bacterial antimicrobial agent susceptibility

Device Story

MicroScan® MICroSTREP plus™ Panel is a miniaturized broth dilution susceptibility test system. Input: bacterial colonies grown on solid media. Process: panels rehydrated with Mueller-Hinton broth supplemented with 2-5% lysed horse blood and 50 mM HEPES; inoculated with standardized organism suspension; incubated 20-24 hours at 35°C +/- 1°C in non-CO2 incubator. Output: visual observation of lowest antimicrobial concentration inhibiting growth (MIC). Used in clinical laboratories by trained personnel. Results assist clinicians in selecting appropriate antimicrobial therapy for streptococcal infections.

Clinical Evidence

Bench testing only. External evaluation compared the MICroSTREP plus™ Panel to an NCCLS frozen Reference Panel using fresh and stock Efficacy isolates and stock Challenge strains. Overall Essential Agreement for Cefotaxime was 98.6%. Reproducibility and quality control testing demonstrated acceptable precision and performance.

Technological Characteristics

Miniaturized broth dilution panel. Materials: Mueller-Hinton broth, 2-5% lysed horse blood, 50 mM HEPES buffer. Energy source: non-CO2 incubator (35°C +/- 1°C). Manual visual reading of growth inhibition. No software or automated algorithm; performance based on standardized broth dilution methodology.

Indications for Use

Indicated for determining quantitative and/or qualitative antimicrobial susceptibility of aerobic streptococci, including Streptococcus pneumoniae, Streptococcus pyogenes (Group A beta-hemolytic streptococci), and Streptococcus agalactiae (Group B streptococci), grown on solid media. Includes testing for Cefotaxime at 0.015-8 mcg/ml.

Regulatory Classification

Identification

An antimicrobial susceptibility test powder is a device that consists of an antimicrobial drug powder packaged in vials in specified amounts and intended for use in clinical laboratories for determining in vitro susceptibility of bacterial pathogens to these therapeutic agents. Test results are used to determine the antimicrobial agent of choice in the treatment of bacterial diseases.

Predicate Devices

• MicroScan® Streptococcus MIC Panel (K963641)

Submission Summary (Full Text)

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#### 6 2002 IIIN

## 510(k) Summary Information:

| Device Manufacturer: | Dade MicroScan Inc. |
|----------------------|----------------------------------------------------------------------------------|
| Contact name: | Cynthia Van Duker, Regulatory Affairs Manager |
| Fax: | 916-374-3144 |
| Date prepared: | April 3, 2002 |
| Product Name: | Microdilution Minimum Inhibitory Concentration (MIC) Panels |
| Trade Name: | MicroScan® MICroSTREP plus™ Panel |
| Intended Use: | To determine bacterial susceptibility to Cefotaxime |
| Indication for Use: | For determining antimicrobic susceptibility with aerobic streptococci, including |
| | <i>Streptococcus pneumoniae</i> |
| Predicate device: | MicroScan® Streptococcus MIC Panel (K963641) |

## 510(k) Summarv:

The MicroScan® MICroSTREP plus™ Panel is used to determine quantitative and/or qualitative antimicrobial agent susceptibility of colonies grown on solid media of aerobic streptococci, including Streptococcus pneumoniae. After inoculation, panels are incubated for 20 - 24 hours at 35°C +/- 1°C in a non-CO2 incubator, and read visually according to the Package Insert.

The antimicrobial susceptibility tests are miniaturizations of the broth dilution susceptibility test. Various antimicrobial agents are diluted in water, buffer or minute concentrations of broth to concentrations bridging the range of clinical interest. Panels are rehydrated with 115 ul Mueller-Hinton broth supplemented with 2-5% lysed horse blood (LHB) and buffered with 50 mM HEPES, after inoculation of the broth with a standardized suspension of the organism in saline. After incubation in a non-CO2 incubator for 20-24 hours, the minimum inhibitory concentration (MIC) for the test organism is manually read by observing the lowest antimicrobial concentration showing inhibition of growth.

The proposed MicroScan® MICroSTREP plus™ Panel demonstrated substantially equivalent performance with streptococcal isolates when compared with an NCCLS frozen Reference Panel, as defined in the FDA DRAFT document "Guidance on Review Criteria for Assessment of Antimicrobial Susceptibility Devices", dated March 8, 2000.

The Premarket Notification (510[k]) presents data in support of the new MCcoSTREP plus™ Panel with Cefotaxime.

The external evaluation was conducted with fresh and stock Efficacy isolates and stock Challenge strains. The external evaluations were designed to confirm the acceptability of the proposed MICroSTREP plus™ Panel by comparing its performance with an NCCLS frozen Reference panel. The MCroSTREP plus™ Panel demonstrated acceptable performance with an overall Essential Agreement of 98.6% for Cefotaxime when compared with the frozen Reference panel.

Reproducibility testing demonstrated acceptable reproducibility and precision with Cefotaxime.

Quality Control testing demonstrated acceptable results for Cefotaxime.

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# DEPARTMENT OF HEALTH & HUMAN SERVICES

Image /page/1/Picture/1 description: The image shows the logo for the Department of Health & Human Services USA. The logo features a stylized eagle with three stripes forming its body and head. The eagle is encircled by the text "DEPARTMENT OF HEALTH & HUMAN SERVICES USA".

Food and Drug Administration 2098 Gaither Road Rockville MD 20850

### 6 2002 JUN

Ms. Cynthia Van Duker Regulatory Affairs Manager Dade Behring Inc. 1584 Enterprise Boulevard West Sacramento, CA 95691

k021111 Re:

Trade/Device Name: MicroScan® MICroSTREP plus™ Panels Microbial agent: Cefotaxime 0.15-8ug/ml Regulation Number: 21 CFR 866.1640 Regulation Name: Antimicrobial Susceptibility Test System Regulatory Class: Class II Product Code: LTT Dated: April 3, 2002 Received: April 5, 2002

Dear Ms. Van Duker:

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. 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.

If your device is classified (see above) into either class II (Special Controls) or class III (PMA), it may be subject to such 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.

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); good manufacturing practice requirements as set forth in the quality systems (QS) regulation (21 CFR Part 820); and if applicable, the electronic product radiation control provisions (Sections 531-542 of the Act); 21 CFR 1000-1050.

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This letter will allow you to begin marketing your device as described in your 510(k) premarket notification. The FDA finding of substantial equivalence of your device to a legally marketed predicate device results in a classification for your device and thus, permits your device to proceed to the market.

If you desire specific advice for your device on our labeling regulation (21 CFR Part 801 and v additionally 809.10 for in vitro diagnostic devices), please contact the Office of Compliance at [phone]. Additionally, for questions on the promotion and advertising of your device, please contact the Office of Compliance at [phone]. Also, please note the regulation entitled, "Misbranding by reference to premarket notification" (21CFR 807.97). Other general information on your responsibilities under the Act may be obtained from the Division of Small Manufacturers International and Consumer Assistance at its toll-free number [phone] or [phone] or at its internet address "http://www.fda.gov/cdrb/dsma/dsmamain.html".

Sincerely yours,

Steven Butman

Steven I. Gutman, M.D., M.B.A. Director Division of Clinical Laboratory Devices Office of Device Evaluation Center for Devices and Radiological Health

Enclosure

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| 510(k) No.: | K021111<br>(To be assigned by FDA) |
|----------------------|------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------|
| Device Name: | MicroScan® MICroSTREP plus™ Panel |
| Intended Use | To determine bacterial antimicrobial agent susceptibility |
| Indications for Use: | The MicroScan® MICroSTREP plus™ Panel is used to determine quantitative and/or qualitative antimicrobial agent susceptibility of colonies grown on solid media of aerobic streptococci, including <i>Streptococcus pneumoniae</i> . After inoculation, panels are incubated for 20 - 24 hours at 35°C +/- 1°C in a non-CO2 incubator, and read visually according to the Package Insert. |
| | This particular submission is for the addition of the antimicrobial Cefotaxime at concentrations of 0.015 to 8 mcg/ml to the test panel |
| | The organisms which may be used for Cefotaxime susceptibility testing in this panel are: |
| | <i>Streptococcus pyogenes</i> (Group A beta-hemolytic streptococci)<br><i>Streptococcus agalactiae</i> (Group B streptococci)<br><i>Streptococcus pneumoniae</i> (formerly <i>Diplococcus pneumoniae</i> ) |

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| | Concurrence of CDRH, Office of Device Evaluation (ODE) | 1 - |
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| | (Division Sign-Cit)<br>Division of Clini. In Laboratory Devices | |
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| | 510(k) Number | |
| Prescription Use_ | | Over-The-Counter Use |
| (Per 21 CFR 801.109) | OR | |
| | | (Optional Format 1-2-96) |