Advantage Thc/Cocaine Test

FDA 510(k) K003708 · Advantage Diagnostics Corp.

Substantially Equivalent

510(k) numberK003708

Submission

Device name
Advantage Thc/Cocaine Test
Applicant
Advantage Diagnostics Corp.
Redwood City, CA, US
Received
December 1, 2000
Decision date
January 22, 2001
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
DIO – Enzyme Immunoassay, Cocaine And Cocaine Metabolites
Device class
Class II (moderate risk)
Regulation
21 CFR 862.3250
Specialty
Clinical Toxicology

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K211973DRI Cocaine Metabolite AssayDIO · Traditional Microgenics Corporation09/24/2021SE
K191638Pointe Scientific Cocaine Metabolite Enzyme ImmunoassayDIO · Traditional Medtest DX03/12/2020SE
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K170293Emit II Plus Cocaine Metabolite AssayDIO · Traditional Siemens Healthcare Diagnostics, Inc.10/25/2017SE
K163570Carolina Liquid Chemistries Cocaine and Cocaine Metabolite Test System (COCM)DIO · Traditional Carolina Liquid Chemistries Corporation08/15/2017SE
K162395MP DOA-10 Panel Test Cup, MP DOA-11 Panel Test CupDIO · Special Mp Biomedicals, LLC06/02/2017SE
K152232Quest Diagnostics HairCheck-DT (Cocaine)DIO · Traditional Quest Diagnostics Incorporated11/18/2016SE
K161214Wondfo Amphetamine Urine Test AMP 500 (Cup, Dipcard), Wondfo Cocaine Urine Test COC…DIO · Traditional Guangzhou Wondfo Biotech Co., Ltd.06/27/2016SE
K153646SAFECARE Urine Test Amphetamine, SAFECARE Urine Test Cocaine, SAFECARE Urine Test…DIO · Traditional Safecare Biotech (Hangzhou) Co., Ltd.03/18/2016SE

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Questions and answers

When was Advantage Thc/Cocaine Test cleared by the FDA?

Advantage Thc/Cocaine Test (K003708) received a 510(k) decision of Substantially Equivalent on January 22, 2001, 52 days after the submission was received.

What is the product code of K003708?

The FDA product code is DIO – Enzyme Immunoassay, Cocaine And Cocaine Metabolites, a Class II (moderate risk) device regulated under 21 CFR 862.3250.