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FDA 510(k)

INORGANIC PHOSPHORUS

K-Number: K874472 · 1987-12-22

ApplicantCatachem, Inc.
Decision Date1987-12-22
Product CodeCEO
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

INORGANIC PHOSPHORUS is the device name listed in this FDA 510(k) record. The listed applicant is Catachem, Inc.. It received FDA 510(k) clearance on 1987-12-22 under 510(k) number K874472. 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 INORGANIC PHOSPHORUS?

INORGANIC PHOSPHORUS is a medical device that received FDA 510(k) clearance on 1987-12-22. The listed applicant is Catachem, Inc.. The 510(k) number is K874472.

When did INORGANIC PHOSPHORUS receive FDA 510(k) clearance?

INORGANIC PHOSPHORUS received FDA 510(k) clearance on 1987-12-22, under 510(k) number K874472.

Who is the listed applicant for INORGANIC PHOSPHORUS?

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

What is the FDA product code for INORGANIC PHOSPHORUS?

The FDA product code for INORGANIC PHOSPHORUS is CEO.

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Other records listing Catachem, 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.

K062503CATACHEM, INC., BILE ACIDS REAGENTS AND/OR BILE ACIDS TEST KITK945408340-CHLORIDE FOR DISCRETE RANDOM ACCESS ANALYZERK932871UIBC FOR DISCREET RANDOM ACCESS ANALYZERK903341MAGNESIUMK902326AMYLASE FOR MANUAL/AUTOMATED APPLICATIONSK902877TOTAL IRON FOR MANUAL/AUTOMATED

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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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