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

SGOT/AST REAGENT SYSTEM

K Number: K780443 · Decision Apr 24, 1978
Classifications
1
FEI Numbers
53
Registration Numbers
53
Same Product Code
138
Applicant Total
73
Review Days
35

Basic Information

Device Name
SGOT/AST REAGENT SYSTEM
K Number
K780443
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
862.1100
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Applicant
AMERICAN MONITOR CORP.
Date Received
March 20, 1978
Decision Date
April 24, 1978
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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K Number Device Name
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K895423 ACCESS CHEMISTRY ANALYZER
K893137 EXCEL (TM) CHEMISTRY ANALYZER
K892331 ENZYMATIC UREA NITROGEN REAGENT SET
K893479 CHOLESTEROL REAGENT SET
K892002 NEOCHROME(R) III GLUCOSE
K890312 GAMMA-GLUTAMYLTRANSFERASE
K890034 PHOTOMETRIC METHOD, IRON (NON-HEME) (75JIY)
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