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

ROCHE REAGENT FOR DIRECT BILIRUBIN

K Number: K910593 · Decision Apr 24, 1991
Classifications
1
FEI Numbers
49
Registration Numbers
49
Same Product Code
234
Applicant Total
296
Review Days
71

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Basic Information

Device Name
ROCHE REAGENT FOR DIRECT BILIRUBIN
K Number
K910593
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
862.1110
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Applicant
Roche Diagnostic Systems, Inc.
Date Received
February 12, 1991
Decision Date
April 24, 1991
Product Code
CIG
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
CIG Diazo Colorimetry, Bilirubin

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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
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