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

BIOTROL AST/TGO MONOREACTIF

K Number: K872829 · Decision Aug 13, 1987
Classifications
1
FEI Numbers
50
Registration Numbers
50
Same Product Code
138
Applicant Total
46
Review Days
27

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Basic Information

Device Name
BIOTROL AST/TGO MONOREACTIF
K Number
K872829
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
862.1100
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Applicant
Biotrol, USA, Inc.
Date Received
July 17, 1987
Decision Date
August 13, 1987
Product Code
CIT
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
CIT Nadh Oxidation/Nad Reduction, Ast/Sgot

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K921677 BIOTROL MAGNESIUM (MAGON)
K912795 BIOTROL UIBC REAGENT
K910721 BIOTROL PROTEIN MULTILEVEL STANDARDS
K905683 BIOTROL LACTATE DEHYDROGENASE (L-P)
K905280 BIOTROL BILIRUBIN C & T CONTROL
K894544 BIOTROL RUB-E.I.A. TEST G
K891061 BIOTROL CALCIUM MONOREACTIF
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