Labeling Change Coat-A-Count Cocaine Metabolite

FDA 510(k) K873751 · Diagnostic Products Corp.

Substantially Equivalent

510(k) numberK873751

Submission

Device name
Labeling Change Coat-A-Count Cocaine Metabolite
Applicant
Diagnostic Products Corp.
Los Angeles, CA, US
Received
September 4, 1987
Decision date
October 15, 1987
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

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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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
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Questions and answers

When was Labeling Change Coat-A-Count Cocaine Metabolite cleared by the FDA?

Labeling Change Coat-A-Count Cocaine Metabolite (K873751) received a 510(k) decision of Substantially Equivalent on October 15, 1987, 41 days after the submission was received.

What is the product code of K873751?

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