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

URIC ACID REAGENT

K Number: K970867 · Decision Apr 21, 1997
Classifications
1
FEI Numbers
53
Registration Numbers
53
Same Product Code
117
Applicant Total
18
Review Days
42

Basic Information

Device Name
URIC ACID REAGENT
K Number
K970867
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
862.1775
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
DERMA MEDIA LAB., INC.
Date Received
March 10, 1997
Decision Date
April 21, 1997
Product Code
KNK
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
KNK Acid, Uric, Uricase (Colorimetric)

Similar 510(k) Clearances

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Other Clearances by DERMA MEDIA LAB., INC.

K Number Device Name
K971309 UREA
K970664 GLUCOSE REAGENT
K971072 CHOLESTEROL REAGENT
K971005 TRIGLYCERIDES
K964915 MAGNESIUM
K964913 IRON REAGENT
K965134 ALT/SGPT
K964914 ALKALINE PHOSPHATASE
K965126 AST/SGOT
K964916 GAMMA-GLUTAMYL TRANSPEPTIDASE
Search all 18 clearances from DERMA MEDIA LAB., INC. →