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

BENZODIAZEPINES/TRICYCLIC ANTIDEPRESSANTS BY HPLC

K Number: K896744 · Decision Feb 23, 1990
Classifications
1
FEI Numbers
90
Registration Numbers
90
Same Product Code
89
Applicant Total
319
Review Days
85

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Basic Information

Device Name
BENZODIAZEPINES/TRICYCLIC ANTIDEPRESSANTS BY HPLC
K Number
K896744
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
862.3170
Medical Specialty
Clinical Toxicology
Decision
Substantially Equivalent
Applicant
Bio-Rad
Date Received
November 30, 1989
Decision Date
February 23, 1990
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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