FDA 510(k) FDA class 1 Substantially Equivalent 🇺🇸 United States

ROCHE REAGENT FOR TRIGLYCERIDES

K Number: K893973 · Decision Aug 11, 1989
Classifications
1
FEI Numbers
39
Registration Numbers
39
Same Product Code
150
Applicant Total
296
Review Days
70

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Basic Information

Device Name
ROCHE REAGENT FOR TRIGLYCERIDES
K Number
K893973
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
862.1705
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Applicant
Roche Diagnostic Systems, Inc.
Date Received
June 2, 1989
Decision Date
August 11, 1989
Product Code
CDT
Advisory Committee
Clinical Chemistry
Review Advisory Committee
CH
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
CDT Lipase Hydrolysis/Glycerol Kinase Enzyme, Triglycerides

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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
K983697 MODIFICATION TO ABUSCREEN ONLINE COCAINE METABOLITE
K983700 MODIFICATION TO ABUSCREEN ONLINE FOR PROPOXYPHENE
K983701 MODIFICATION TO ABUSCREEN ONLINE FOR CANNABINOIDS
K983699 MODIFICATION TO ABUSCREEN ONLINE FOR AMPHETAMINES
K983703 MODIFICATION TO ABUSCREEN ONLINE FOR METHADONE
Search all 296 clearances from Roche Diagnostic Systems, Inc. →