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

ACCU-CHEK EASY BLOOD GLUCOSE SYSTEM

K Number: K923048 · Decision Oct 14, 1992
Classifications
1
FEI Numbers
145
Registration Numbers
145
Same Product Code
399
Applicant Total
340
Review Days
112

Basic Information

Device Name
ACCU-CHEK EASY BLOOD GLUCOSE SYSTEM
K Number
K923048
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
862.1345
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
BOEHRINGER MANNHEIM CORP.
Date Received
June 24, 1992
Decision Date
October 14, 1992
Product Code
CGA
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
CGA Glucose Oxidase, Glucose

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