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

CREATINE KINASE FOR MANUAL/AUTOMATED APPLICATIONS

K Number: K894715 · Decision Nov 8, 1989
Classifications
1
FEI Numbers
25
Registration Numbers
25
Same Product Code
122
Applicant Total
41
Review Days
106

Research this 510(k) in seconds

The Research Assistant summarizes clearance history, predicates and product-code trends — and cites every record.

Free to try · every answer cites its records

Basic Information

Device Name
CREATINE KINASE FOR MANUAL/AUTOMATED APPLICATIONS
K Number
K894715
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
862.1215
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Applicant
Catachem, Inc.
Date Received
July 25, 1989
Decision Date
November 8, 1989
Product Code
CGS
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
CGS Nad Reduction/Nadh Oxidation, Cpk Or Isoenzymes

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (CGS), ordered by most recent decision date.

View all

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
K895821 URIC ACID 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. →