Atlas FDA

Psychemedics Microplate EIA for Cotinine in Hair

FDA 510(k) clearance K192517 · decided 2020-04-22

Clearance details

K-number
K192517
Device name
Psychemedics Microplate EIA for Cotinine in Hair
Applicant
Psychemedics Corporation
Decision
Substantially Equivalent
Date received
2019-09-13
Decision date
2020-04-22
Days to decision
222 days
Clearance type
Traditional
Product code
MKU
Device class
1
Regulation number
862.3220
Medical specialty
Clinical Toxicology
Advisory committee
Clinical Toxicology
Location
Culver City, CA, US
Third-party review
No
Expedited review
No

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Similar devices under this product code

Devices cleared under the same product code - the starting set for predicate research.

RecordFirmDate
LZI Cotinine II Enzyme Immunoassay (K192299)Lin-Zhi International, Inc.2019-11-21
STATUS DS NICOTINE, ACCUSIGN NICOTINE, BIOSIGN NICOTINE (K062565)Princeton BioMeditech Corp.2007-02-20
COZART EIA COTININE URINE KIT (K021944)Cozart Bioscience , Ltd.2003-05-14
MICRO-PLATE COTININE EIA (K974534)OraSure Technologies, Inc.1998-05-18
MICRO-PLATE COTININE EIA (K974234)OraSure Technologies, Inc.1998-05-14
AUTO-LYTE COTININE EIA (K972481)OraSure Technologies, Inc.1997-10-21

Recalls involving this device

No recalls on record reference this clearance.