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

COBAS-FP REAGENT FOR VALPROIC ACID AND CALIBRATORS

K Number: K925003 · Decision Dec 3, 1992
Classifications
1
FEI Numbers
26
Registration Numbers
26
Same Product Code
34
Applicant Total
296
Review Days
62

Basic Information

Device Name
COBAS-FP REAGENT FOR VALPROIC ACID AND CALIBRATORS
K Number
K925003
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
862.3645
Medical Specialty
Clinical Toxicology
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
ROCHE DIAGNOSTIC SYSTEMS, INC.
Date Received
October 2, 1992
Decision Date
December 3, 1992
Product Code
LEG
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
LEG Enzyme Immunoassay, Valproic Acid

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (LEG), ordered by most recent decision date.

View all

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. →