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

ABUSCREEN(R) ONLINE(TM) FOR BENZODIAZEPINES

K Number: K914509 · Decision Nov 1, 1991
Classifications
1
FEI Numbers
94
Registration Numbers
94
Same Product Code
89
Applicant Total
296
Review Days
23

Basic Information

Device Name
ABUSCREEN(R) ONLINE(TM) FOR BENZODIAZEPINES
K Number
K914509
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
862.3170
Medical Specialty
Clinical Toxicology
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
ROCHE DIAGNOSTIC SYSTEMS, INC.
Date Received
October 9, 1991
Decision Date
November 1, 1991
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 ROCHE DIAGNOSTIC SYSTEMS, INC.

K Number Device Name
K983698 MODIFICATION TO ABUSCREEN ONLINE BARBITURATES
K983702 MODIFICATION TO ABUSCREEN ONLINE FOR BENZOIDIAZEPINES
K983704 MODIFICATION TO ABUSCREEN ONLINE FOR PHENCYCLIDINE
K983556 ABUSCREEN ONLINE BENZ 300 CALIBRATORS
K983555 ABUSCREEN ONLINE BENZ 200 CALIBRATORS
K983700 MODIFICATION TO ABUSCREEN ONLINE FOR PROPOXYPHENE
K983697 MODIFICATION TO ABUSCREEN ONLINE COCAINE METABOLITE
K983699 MODIFICATION TO ABUSCREEN ONLINE FOR AMPHETAMINES
K983703 MODIFICATION TO ABUSCREEN ONLINE FOR METHADONE
K983701 MODIFICATION TO ABUSCREEN ONLINE FOR CANNABINOIDS
Search all 296 clearances from ROCHE DIAGNOSTIC SYSTEMS, INC. →