FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

CEDIA Heroin Metabolite (6-AM) assay

K Number: K192943 · Decision Dec 16, 2019
Classifications
1
FEI Numbers
100
Registration Numbers
100
Same Product Code
214
Applicant Total
21
Review Days
59

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Basic Information

Device Name
CEDIA Heroin Metabolite (6-AM) assay
K Number
K192943
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
862.3650
Medical Specialty
Clinical Toxicology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Microgenics Corporation
Date Received
October 18, 2019
Decision Date
December 16, 2019
Product Code
DJG
Advisory Committee
Clinical Toxicology
Review Advisory Committee
TX
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
DJG Enzyme Immunoassay, Opiates

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Other Clearances by Microgenics Corporation

K Number Device Name
K243498 Alinity c Benzodiazepines Reagent Kit
K240670 DRI Ecstasy Plus Assay
K231020 Alinity c Tricyclic Antidepressants Reagent Kit
K231007 CEDIA Heroin Metabolite (6-AM) Assay
K213875 DRI TM Tricyclics Serum Tox Assay
K211973 DRI Cocaine Metabolite Assay
K190968 CEDIA Benzodiazepine Assay
DEN180030 QMS Plazomicin Immunoassay
K181499 DRI Cocaine Metabolite Assay
K173963 DRI Benzodiazepine Assay
Search all 21 clearances from Microgenics Corporation →