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

ADX TM BENZODIAZEPINES

K Number: K890691 · Decision Aug 25, 1989
Classifications
1
FEI Numbers
90
Registration Numbers
90
Same Product Code
89
Applicant Total
883
Review Days
192

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Basic Information

Device Name
ADX TM BENZODIAZEPINES
K Number
K890691
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
862.3170
Medical Specialty
Clinical Toxicology
Decision
Substantially Equivalent
Applicant
Abbott Laboratories
Date Received
February 14, 1989
Decision Date
August 25, 1989
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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