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

ALKALINE PHOSPHATASE (AP) FOR CONT. FLOW INSTRU.

K Number: K871543 · Decision Jun 22, 1987
Classifications
1
FEI Numbers
37
Registration Numbers
37
Same Product Code
123
Applicant Total
41
Review Days
63

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Basic Information

Device Name
ALKALINE PHOSPHATASE (AP) FOR CONT. FLOW INSTRU.
K Number
K871543
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
862.1050
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Applicant
Catachem, Inc.
Date Received
April 20, 1987
Decision Date
June 22, 1987
Product Code
CJE
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
CJE Nitrophenylphosphate, Alkaline Phosphatase Or Isoenzymes

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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
K895821 URIC ACID FOR MANUAL/AUTOMATED APPLICATIONS
K894715 CREATINE KINASE FOR MANUAL/AUTOMATED APPLICATIONS
K894389 CREATININE FOR MANUAL OR AUTOMATED APPLICATIONS
Search all 41 clearances from Catachem, Inc. →