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

GLUCOSE-HK SYSTEM PACK TEST

K Number: K812303 · Decision Sep 1, 1981
Classifications
1
FEI Numbers
45
Registration Numbers
45
Same Product Code
144
Applicant Total
340
Review Days
14

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Basic Information

Device Name
GLUCOSE-HK SYSTEM PACK TEST
K Number
K812303
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
862.1345
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Applicant
Boehringer Mannheim Corp.
Date Received
August 18, 1981
Decision Date
September 1, 1981
Product Code
CFR
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
CFR Hexokinase, Glucose

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