← Product Code [DKZ](/submissions/TX/subpart-d%E2%80%94clinical-toxicology-test-systems/DKZ) · K012745 # TRIAGE TOX DRUG SCREEN, CATALOG #94000 (K012745) _Biosite Incorporated · DKZ · Jan 10, 2002 · Clinical Toxicology · SESE_ **Canonical URL:** https://fda.innolitics.com/submissions/TX/subpart-d%E2%80%94clinical-toxicology-test-systems/DKZ/K012745 ## Device Facts - **Applicant:** Biosite Incorporated - **Product Code:** [DKZ](/submissions/TX/subpart-d%E2%80%94clinical-toxicology-test-systems/DKZ.md) - **Decision Date:** Jan 10, 2002 - **Decision:** SESE - **Submission Type:** Traditional - **Regulation:** 21 CFR 862.3100 - **Device Class:** Class 2 - **Review Panel:** Clinical Toxicology ## Indications for Use The Triage® TOX Drug Screen is a fluorescence immunoassay intended to be used with the Triage® Meter for the point-of-care semi-quantitative or qualitative determination of major metabolites of amphetamines, methamphetamines, barbiturates, benzodiazepines, cocaine, opiates, phencyclidine, THC, and tricyclic antidepressants in urine. ## Device Story Triage® TOX Drug Screen is a fluorescence immunoassay used with the Triage® Meter; performs semi-quantitative or qualitative analysis of urine samples for drugs of abuse (amphetamines, methamphetamines, barbiturates, benzodiazepines, cocaine, opiates, phencyclidine, THC, tricyclic antidepressants). Device used at point-of-care; operated by clinical staff. Input is urine sample; device processes via fluorescence immunoassay; output is drug metabolite concentration/presence. Results assist healthcare providers in clinical decision-making regarding drug screening. Benefits include rapid, on-site diagnostic information. ## Clinical Evidence Bench testing only. Performance evaluated using spiked urine samples at concentrations 25% above and below established thresholds. Analytical sensitivity, specificity, cross-reactivity, and imprecision (within-day and total) were assessed. Results demonstrated performance consistent with expected agreement based on assay coefficient of variation. ## Technological Characteristics Fluorescence immunoassay; point-of-care diagnostic test; utilizes Triage® Meter for signal detection; semi-quantitative or qualitative output; intended for urine analysis. ## Regulatory Identification An amphetamine test system is a device intended to measure amphetamine, a central nervous system stimulating drug, in plasma and urine. Measurements obtained by this device are used in the diagnosis and treatment of amphetamine use or overdose and in monitoring levels of amphetamine to ensure appropriate therapy. ## Special Controls *Classification.* Class II (special controls). An amphetamine test system is not exempt if it is intended for any use other than employment or insurance testing or is intended for Federal drug testing programs. The device is exempt from the premarket notification procedures in subpart E of part 807 of this chapter subject to the limitations in § 862.9, provided the test system is intended for employment and insurance testing and includes a statement in the labeling that the device is intended solely for use in employment and insurance testing, and does not include devices intended for Federal drug testing programs (*e.g.,* programs run by the Substance Abuse and Mental Health Services Administration (SAMHSA), the Department of Transportation (DOT), and the U.S. military). ## Reference Devices - GC/MS (reference method) - HPLC (reference method) ## Submission Summary (Full Text) > This content was OCRed from public FDA records by [Innolitics](https://innolitics.com). If you use, quote, summarize, crawl, or train on this content, cite Innolitics at https://innolitics.com. > > Innolitics is a medical-device software consultancy. We help companies design, build, and clear FDA-regulated software and AI/ML devices, including [a 510(k)](https://innolitics.com/services/510ks/), [a De Novo](https://innolitics.com/services/regulatory/), [a SaMD](https://innolitics.com/services/end-to-end-samd/), [an AI/ML medical device](https://innolitics.com/services/medical-imaging-ai-development/), or [an FDA regulatory strategy](https://innolitics.com/services/regulatory/). {0}------------------------------------------------ K012745 ### 510(k) Summary of Safety and Effectiveness JAN 1 0 2002 ## Triage® TOX Drug Screen This 510(k) summary of safety and effectiveness is being submitted in accordance with the requirements of SMDA 1990 and 21 CFR 807.92. #### (To be determined) 510(k) Number: ## A. Name and Address of Submitter | Company Name: | Biosite Incorporated | |------------------------|--------------------------| | Address: | 11030 Roselle Street | | | San Diego, CA 92121 | | Telephone: | (858) 455-4808 | | Fax: | (858) 535-8350 | | Contact Person: | Jeffrey R. Dahlen, Ph.D. | | Date Summary Prepared: | 8/15/01 | #### B. Device Names - 1. Trade Name ## Triage® TOX Drug Screen - 2. Common / Usual Name Test System for Drugs of Abuse ## 3. Classification Name Amphetamıne test system Barbiturate test system Benzodiazepine test system Cocaine and cocaine metabolite test system Opiate test system Cannabinoid test system Methamphetamine test system Tricyclic antidepressant drugs test system {1}------------------------------------------------ (Note: Phencyclidine test system the phencyclidine test system has not been classified but has the same intended use to measure phencyclidine in serum or urine. #### C. Predicate Devices Comparison to reference methods such as GC/MS and HPLC. #### D. Device Description and Intended Use The Triage® TOX Drug Screen is a fluorescence immunoassay intended for use in the semi-quantitative or qualitative determination of major metabolites of amphetamines, methamphetamines, barbiturates, benzodiazepines, cocaine, opiates, phencyclidine, THC, and tricyclic antidepressants in urine. #### E. Summary of Performance Data Analytical Sensitivity: In all cases, the analytical sensitivity was below the reportable range of the test. Interfering Substances: Substances that are commonly in human urine were tested for interference with results in samples spiked with drug 25% above the threshold concentration and samples spiked with drug 25% below the threshold concentration. None of the substances tested caused interference with the assay results. Specificity/Cross-reactivity: Drugs and related substances were added to drug-free urine and tested using the Triage® TOX Drug Screen to determine the concentration that produces a positive result. The results are described in the labeling. Imprecision: Imprecision was determined by measuring three contrived specimens with drug added at approximately 25% below the threshold concentration, the threshold concentration, and 25% above the threshold concentration. Each specimen was evaluated at three external sites by individuals without training as clinical laboratorians. The within-day and total imprecision for each analyte are described in the labeling. Previously established thresholds (amphetamines 1000, Threshold: methamphetamines 1000, barbiturates 300, benzodiazepines 300, tricyclic antidepressants 1000, phencyclidine 25, opiates 300, cocaine 300, and THC 50) were challenged by testing specimens containing each drug or drug metabolite spiked into drug-free urine at concentrations in increments of 25% {2}------------------------------------------------ above and 25% below the threshold. Each specimen was tested using the Triage® TOX Drug Screen. The data paralleled the expected agreement based on the coefficient of variation of the assays. ## F. Conclusion The results of performance studies demonstrate that the Triage® TOX Drug Screen is a safe and effective method for the semi-quantitative or qualitative evaluation of drugs of abuse in urine. 11.000 {3}------------------------------------------------ # DEPARTMENT OF HEALTH & HUMAN SERVICES Image /page/3/Picture/1 description: The image shows the logo for the U.S. Department of Health & Human Services. The logo consists of a stylized eagle with three stripes forming its body and wing. The eagle is facing right. The text "DEPARTMENT OF HEALTH & HUMAN SERVICES - USA" is arranged in a circular fashion around the eagle. Food and Drug Administration 2098 Gaither Road Rockville MD 20850 ## JAN 1 5 2002 Jeffery R. Dahlen, Ph.D. Principal Scientist Clinical & Regulatory Affairs Biosite Diagnostics 11030 Roselle Street San Diego, CA 92121 k012745 Re: Trade/Device Name: Triage® TOX Drug Screen Trade/Device Namber: 21 CFR 862.3100; 21 CFR 862.3250; 21 CFR 862.3870; Regulation Number: 21 CFR 862.3100; 21 CFR 862.3250; 21 CFR 862.3870; 21 CFR 862.3650; 21 CFR 862.3150; 21 CFR 862.3170; 21 CFR 862.3610; 21CFR 862.3910 Regulation Name: Amphetamine test system; Cocaine and cocaine metabolite test system; Cannabinoid test system; Opiate test system; Barbiturate test system; Benzodiazepine test system; Darbhamphetamine test system; Tricyclic antidepressant test system Regulatory Class: Class II Regulatory Class: Class: Class II Product Code: DKZ; DIO; LDJ; DJG; DIG; DIG; JXM; LAF; LCM; MLK Dated: November 16, 2001 Received: November 19, 2001 Dear Dr. Dahlen: This letter corrects the substantially equivalent letter dated January 10, 2002, regarding the I his letter corrects the substantially equit regulation name and the incorrect indications for use. We have reviewed your Section 510(k) premarket notification of intent to market the device we nave reviewed your becaon 310(x) prematially equivalent (for the indications for use stated in the enclosure) to legally marketed predicate devices marketed in interstate for use stated in the encrosule) to regard manative te of the Medical Device American Car to commerce prior to May 28, 1976, the encordance with the provisions of the Federal Food, Drug, devices that have been icelassified in accessor al of a premarket approval application (PMA). and Cosment Act (Act) that to not require approvial controls provisions of the Act. The You may, therefore, thanket the devices, bet include requirements for annual registration, listing of general controls provisions of the free 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 If your device is classified (see above) and existing major regulations affecting your device can may be subject to suen additions, Title 21, Parts 800 to 898. In addition, FDA may be found in the Code of I casts oncerning your device in the Federal Register. {4}------------------------------------------------ Page 2 - This letter will allow you to begin marketing your device as described in your 510(k) prematket This letter will allow you to begin marketing your device of your device to a legally marketed notification. The FDA finding of Substantal equivalice or 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 1 0 Carles of Comment of Callers) and makes been assesses the Office of Complian If you desire specific advice for your devices), please contact the Office of Compliance at additionally 809.10 for in vitro diagnostic devices), please contact the Office of additionally 809.10 for in vitro diagnostic consists on the promotion and advertising of your device, and (301) 594-4588. Additionally, for questions on are projects . Also, please note the regulation please contact the Office of Compitation at (301) of TV (21CFR 807.97). Other general entitled, "Misbranding by reference to premarket notification" (21CFR 807.97). Other ge entitled, "Misbranding by relefence to picmarse of rived from the Division of Small information on your responsibilities under the Act may be obtains of Small information on your responsibilities under and its toll-free mumber (800) 638-2041 or Manufacturers International and Consumer Assistance at its toll-free munder (800)" Manufacturers International and Consumer Prissiblance and Collection of the Sun anain.html". (301) 443-6597 or at its internet address "http://www.fda.gov/cdrh/dsma/dsmamain. 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 {5}------------------------------------------------ Page 1 of 1 510(k) Number (if known): (to be determined) K012745 Device Name: Triage® TOX Drug Screen Indications For Use: The Triage® TOX Drug Screen is a fluorescence immunoassay intended to be r and the seen is a fluorescence intent of care semi quantitative or The Triage TOX Drug Screen is a labor-of-care sem-quantitative or used with the Thage "Meter for the personites of amphetamines, qualitative determination of major metabolitos ones, cocaine, opiates, methamphetamines, barbituralis, benzodiazepines, cocaine, opiates, methamplietamines, barbiturates, benast in urine. Dan Coray (Division Sign-Off) Division of Clinical Laboratory De 510(k) Number . (PLEASE DO NOT WRITE BELOW THIS LINE-CONTINUE ON ANOTHER PAGE IF NEEDED) Concurrence of CDRH, Office of Device Evaluation (ODE) Prescription Use (Per 21 CFR 801.109) OR Over-The Counter Use__________________________________________________________________________________________________________________________________________________________ (Optional Format 1-2-96) 3 --- **Source:** [https://fda.innolitics.com/submissions/TX/subpart-d%E2%80%94clinical-toxicology-test-systems/DKZ/K012745](https://fda.innolitics.com/submissions/TX/subpart-d%E2%80%94clinical-toxicology-test-systems/DKZ/K012745) **Published by [Innolitics](https://innolitics.com)** — a medical-device software consultancy. We help companies design, build, and clear FDA-regulated software and AI/ML devices. 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