Drugs of Abuse Multi-Test Strip

FDA 510(k) K011952 · Microdiagnostics, Inc.

Substantially Equivalent

510(k) numberK011952

Submission

Device name
Drugs of Abuse Multi-Test Strip
Applicant
Microdiagnostics, Inc.
Laguna Niguel, CA, US
Received
June 21, 2001
Decision date
October 25, 2001
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) statement available from FDA

Official FDA 510(k) record

Device classification

Product code
DKZ – Enzyme Immunoassay, Amphetamine
Device class
Class II (moderate risk)
Regulation
21 CFR 862.3100
Specialty
Clinical Toxicology

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More from Alfa Scientific Designs, Inc.

510(k)DeviceDecision
K991516Micro-Strip for Marijuana MetabolitesLDJ · Traditional 08/05/1999SE
K991505Micro-Strip for Phencyclidine MetabolitesLCM · Traditional 08/05/1999SE
K981388Micro-Strip for Cocaine MetabolitesDIO · Traditional 05/29/1998SE
K974611Micro-Strip for Amphetamine MetabolitesDKZ · Traditional 03/20/1998SE
K973761Micro-Strip for Opiate MetabolitesDJG · Traditional 12/24/1997SE
K932304Micro Eia for Amphetamine MetabolitesDKZ · Traditional 12/07/1993SE
K923468Micro Eia for Opiate MetabolitesDJG · Traditional 09/15/1992SE
K914533Micro Eia for Cocaine MetabolitesDIO · Traditional 12/10/1991SE
K914490Micro Eia for Marijuana MetabolitesLDJ · Traditional 11/29/1991SE

Questions and answers

When was Drugs of Abuse Multi-Test Strip cleared by the FDA?

Drugs of Abuse Multi-Test Strip (K011952) received a 510(k) decision of Substantially Equivalent on October 25, 2001, 126 days after the submission was received.

What is the product code of K011952?

The FDA product code is DKZ – Enzyme Immunoassay, Amphetamine, a Class II (moderate risk) device regulated under 21 CFR 862.3100.