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

URIC ACID FOR MANUAL/AUTOMATED APPLICATIONS

K Number: K895821 · Decision Dec 5, 1989
Classifications
1
FEI Numbers
49
Registration Numbers
49
Same Product Code
117
Applicant Total
41
Review Days
67

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Basic Information

Device Name
URIC ACID FOR MANUAL/AUTOMATED APPLICATIONS
K Number
K895821
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
862.1775
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Applicant
Catachem, Inc.
Date Received
September 29, 1989
Decision Date
December 5, 1989
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)

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Other Clearances by Catachem, Inc.

K Number Device Name
K062503 CATACHEM, INC., BILE ACIDS REAGENTS AND/OR BILE ACIDS TEST KIT
K945408 340-CHLORIDE FOR DISCRETE RANDOM ACCESS ANALYZER
K932871 UIBC FOR DISCREET RANDOM ACCESS ANALYZER
K903341 MAGNESIUM
K902326 AMYLASE FOR MANUAL/AUTOMATED APPLICATIONS
K902877 TOTAL IRON FOR MANUAL/AUTOMATED
K895748 BICARBONATE FOR MANUAL/AUTOMATED APPLICATIONS
K894715 CREATINE KINASE FOR MANUAL/AUTOMATED APPLICATIONS
K894389 CREATININE FOR MANUAL OR AUTOMATED APPLICATIONS
K894476 CALCIUM (ARSENAZO III) FOR MANUAL/AUTO APPLICATION
Search all 41 clearances from Catachem, Inc. →