Psychemedics Homogeneous Enzyme Immunoassay for Amphetamines in Hair

FDA 510(k) K210212 · Psychemedics Corporation

Substantially Equivalent

510(k) numberK210212

Submission

Device name
Psychemedics Homogeneous Enzyme Immunoassay for Amphetamines in Hair
Applicant
Psychemedics Corporation
Culver City, CA, US
Received
January 27, 2021
Decision date
December 15, 2021
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
LAF – Gas Chromatography, Methamphetamine
Device class
Class II (moderate risk)
Regulation
21 CFR 862.3610
Specialty
Clinical Toxicology

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More from Psychemedics Corp.

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K212952Psychemedics Homogeneous Enzyme Immunoassay (HEIA) for Phencyclidine in HairLCM · Traditional 04/18/2022SE
K201326Psychemedics Homogeneous Enzyme Immunoassay (HEIA) for Opiates in Hair, Psychemedics…DJG · Traditional 07/27/2021SE
K201228Psychemedics Homogeneous Enzyme Immunoassay for Cocaine in HairJXO · Traditional 06/25/2021SE
K192517Psychemedics Microplate EIA for Cotinine in HairMKU · Traditional 04/22/2020SE
K182103Psychemedics Microplate EIA for Fentanyl in HairDJG · Traditional 04/18/2019SE
K163590Psychemedics Microplate EIA for Benzodiazepines in HairJXM · Traditional 09/15/2017SE
K130811Psychemedics Microplate Eia for AmphetamineDKZ · Traditional 05/02/2013SE
K123799Psychemedics Microplate Eia for Oxycodone in HairDJG · Traditional 02/08/2013SE
K111929Psychemedics Cannabinoids EiaLDJ · Traditional 05/01/2012SE
K111928Psychemedics Phencyclidine EiaLCM · Traditional 05/01/2012SE

Questions and answers

When was Psychemedics Homogeneous Enzyme Immunoassay for Amphetamines in Hair cleared by the FDA?

Psychemedics Homogeneous Enzyme Immunoassay for Amphetamines in Hair (K210212) received a 510(k) decision of Substantially Equivalent on December 15, 2021, 322 days after the submission was received.

What is the product code of K210212?

The FDA product code is LAF – Gas Chromatography, Methamphetamine, a Class II (moderate risk) device regulated under 21 CFR 862.3610.