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

ALT (GPT) LIQUID STABLE 2 VIAL - INCORPORATING DYNAMIC STABILIZATION TECHNOLOGY - (DST)

K Number: K980028 · Decision Feb 2, 1998
Classifications
1
FEI Numbers
49
Registration Numbers
49
Same Product Code
126
Applicant Total
22
Review Days
28

Basic Information

Device Name
ALT (GPT) LIQUID STABLE 2 VIAL - INCORPORATING DYNAMIC STABILIZATION TECHNOLOGY - (DST)
K Number
K980028
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
862.1030
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
TRACE AMERICA, INC.
Date Received
January 5, 1998
Decision Date
February 2, 1998
Product Code
CKA
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
CKA Nadh Oxidation/Nad Reduction, Alt/Sgpt

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