FDA 510(k) FDA class 1 Substantially Equivalent 🇺🇸 United States

SGPT REAGENT SET

K Number: K820491 · Decision Mar 11, 1982
Classifications
1
FEI Numbers
6
Registration Numbers
6
Same Product Code
10
Applicant Total
26
Review Days
16

Basic Information

Device Name
SGPT REAGENT SET
K Number
K820491
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
862.1030
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Applicant
ANCO MEDICAL REAGENTS & ASSOC.
Date Received
February 23, 1982
Decision Date
March 11, 1982
Product Code
CKD
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
CKD Hydrazone Colorimetry, Alt/Sgpt

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K821526 ACID PHOSPHATASE REAGENT SET
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