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

DRI Benzodiazepine Assay

K Number: K173963 · Decision Feb 21, 2018
Classifications
1
FEI Numbers
90
Registration Numbers
90
Same Product Code
89
Applicant Total
21
Review Days
55

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Basic Information

Device Name
DRI Benzodiazepine Assay
K Number
K173963
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
862.3170
Medical Specialty
Clinical Toxicology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Microgenics Corporation
Date Received
December 28, 2017
Decision Date
February 21, 2018
Product Code
JXM
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
JXM Enzyme Immunoassay, Benzodiazepine

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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
K192943 CEDIA Heroin Metabolite (6-AM) assay
K190968 CEDIA Benzodiazepine Assay
DEN180030 QMS Plazomicin Immunoassay
K181499 DRI Cocaine Metabolite Assay
Search all 21 clearances from Microgenics Corporation →