MULTICHEM INORGANIC PHOSPHOROUS S0923— 510(k) K874038

Name: FDA 510(k) clearance K874038
Creator: U.S. Food and Drug Administration
Published: 1987-10-28

Substantially Equivalent

Simmler, Inc.

FDA 510(k) clearance K874038 for MULTICHEM INORGANIC PHOSPHOROUS S0923, Substantially Equivalent on 1987-10-28. Applicant: Simmler, Inc.. Device class: 1.

Clearance details

Applicant: Simmler, Inc.
Product code: Code CEO
Device class: Class 1
Regulation: 21 CFR 862.1580
Advisory panel: Clinical Chemistry
Date received: 1987-10-05
Decision date: 1987-10-28
Decision: Substantially Equivalent
Clearance type: Traditional
Location: St. Louis, MO, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code CEO

view all

K100263 — ELITECH CLINICAL SYSTEMS PHOSPHORUS, URIC ACID MONO SL AND UREA UV SL REAGENTS2011-05-06
K072141 — S40 CLINICAL ANALYZER, S TEST IP, S TEST UA2008-06-24
K041643 — SYNCHRON SYSTEMS PHOSPHORUS (PHS) REAGENT2004-08-18
K030015 — ATAC PAK PHOSPHORUS REAGENT2003-03-07
K022312 — PICCOLO PHOSPHORUS TEST SYSTEM2002-09-05

More clearances from Simmler, Inc.

view all

K895745 — SICKLE CELL SOLUBILITY TEST KIT1989-11-29
K874903 — MULTICHEM(R) Y -GLUTAMYLTRANSFERASE (Y -GT)1988-02-11
K874595 — MULTICHEM (R) MAGNESIUM REAGENT1988-01-21
K874820 — MULTICHEM HDL PRECIPITATING REAGENT #S09141988-01-07
K874812 — MULTICHEM CHLORIDE REAGENT S09331987-12-18

Data sourced from openFDA. This site is unofficial and independent of the FDA.