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FDA 510(k)

MULTICHEM INORGANIC PHOSPHOROUS S0923

K-Number: K874038 · 1987-10-28

ApplicantSimmler, Inc.
Decision Date1987-10-28
Product CodeCEO
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

MULTICHEM INORGANIC PHOSPHOROUS S0923 is the device name listed in this FDA 510(k) record. The listed applicant is Simmler, Inc.. It received FDA 510(k) clearance on 1987-10-28 under 510(k) number K874038. The device is classified under product code CEO. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MULTICHEM INORGANIC PHOSPHOROUS S0923?

MULTICHEM INORGANIC PHOSPHOROUS S0923 is a medical device that received FDA 510(k) clearance on 1987-10-28. The listed applicant is Simmler, Inc.. The 510(k) number is K874038.

When did MULTICHEM INORGANIC PHOSPHOROUS S0923 receive FDA 510(k) clearance?

MULTICHEM INORGANIC PHOSPHOROUS S0923 received FDA 510(k) clearance on 1987-10-28, under 510(k) number K874038.

Who is the listed applicant for MULTICHEM INORGANIC PHOSPHOROUS S0923?

The FDA 510(k) record lists Simmler, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MULTICHEM INORGANIC PHOSPHOROUS S0923?

The FDA product code for MULTICHEM INORGANIC PHOSPHOROUS S0923 is CEO.

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Other records listing Simmler, Inc. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K895745SICKLE CELL SOLUBILITY TEST KITK874903MULTICHEM(R) Y -GLUTAMYLTRANSFERASE (Y -GT)K874595MULTICHEM (R) MAGNESIUM REAGENTK874820MULTICHEM HDL PRECIPITATING REAGENT #S0914K874812MULTICHEM CHLORIDE REAGENT S0933K874311MULTICHEM (R) TOTAL BILIRUBIN

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Related Devices (Code: CEO)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K100263ELITECH CLINICAL SYSTEMS PHOSPHORUS, URIC ACID MONO SL AND UREA UV SL REAGENTSSeppim S.A.S.K072141S40 CLINICAL ANALYZER, S TEST IP, S TEST UAAlfa Wassermann Diagnostic Technologies, Inc.K041643SYNCHRON SYSTEMS PHOSPHORUS (PHS) REAGENTBeckman Coulter, Inc.K030015ATAC PAK PHOSPHORUS REAGENTElan DiagnosticsK022312PICCOLO PHOSPHORUS TEST SYSTEMAbaxis, Inc.K013095WIENER LAB.FOSFATEMIA UV, MODELS 1X100 ML CAT.N 1382321, 4X20 ML CAT.N 1009311Wiener Laboratories Saic

Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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