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

INORGANIC PHOSPHORUS

K Number: K874472 · Decision Dec 22, 1987
Classifications
1
FEI Numbers
38
Registration Numbers
38
Same Product Code
104
Applicant Total
41
Review Days
50

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
INORGANIC PHOSPHORUS
K Number
K874472
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
862.1580
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Applicant
Catachem, Inc.
Date Received
November 2, 1987
Decision Date
December 22, 1987
Product Code
CEO
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
CEO Phosphomolybdate (Colorimetric), Inorganic Phosphorus

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (CEO), 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
K894715 CREATINE KINASE FOR MANUAL/AUTOMATED APPLICATIONS
K894389 CREATININE FOR MANUAL OR AUTOMATED APPLICATIONS
Search all 41 clearances from Catachem, Inc. →