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

MULTICHEM INORGANIC PHOSPHOROUS S0923

K Number: K874038 · Decision Oct 28, 1987
Classifications
1
FEI Numbers
38
Registration Numbers
38
Same Product Code
104
Applicant Total
23
Review Days
23

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Basic Information

Device Name
MULTICHEM INORGANIC PHOSPHOROUS S0923
K Number
K874038
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
862.1580
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Applicant
Simmler, Inc.
Date Received
October 5, 1987
Decision Date
October 28, 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

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Other Clearances by Simmler, Inc.

K Number Device Name
K895745 SICKLE CELL SOLUBILITY TEST KIT
K874903 MULTICHEM(R) Y -GLUTAMYLTRANSFERASE (Y -GT)
K874595 MULTICHEM (R) MAGNESIUM REAGENT
K874820 MULTICHEM HDL PRECIPITATING REAGENT #S0914
K874812 MULTICHEM CHLORIDE REAGENT S0933
K874311 MULTICHEM (R) TOTAL BILIRUBIN
K874049 MULTICHEM ALBUMIN REAGENT S0902
K873725 MULTICHEM CREATININE REAGENT S0917
K873761 MULTICHEM ALKALINE PHOSPHATASE (S0903)
K873697 MULTICHEM CALCIUM S0910
Search all 23 clearances from Simmler, Inc. →