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

UNITEST AMYLASE

K Number: K782032 · Decision Mar 2, 1979
Classifications
1
FEI Numbers
7
Registration Numbers
7
Same Product Code
7
Applicant Total
340
Review Days
86

Basic Information

Device Name
UNITEST AMYLASE
K Number
K782032
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
862.1070
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Applicant
BOEHRINGER MANNHEIM CORP.
Date Received
December 6, 1978
Decision Date
March 2, 1979
Product Code
CIW
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
CIW Starch-Dye Bound Polymer, Amylase

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