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FDA 510(k)

AMMONIUM MOLYBDATE INORGANIC PHOSPHORUS

K-Number: K802159 · 1980-10-10

ApplicantPanmed, Inc.
Decision Date1980-10-10
Product CodeCEO
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

AMMONIUM MOLYBDATE INORGANIC PHOSPHORUS is the device name listed in this FDA 510(k) record. The listed applicant is Panmed, Inc.. It received FDA 510(k) clearance on 1980-10-10 under 510(k) number K802159. 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 AMMONIUM MOLYBDATE INORGANIC PHOSPHORUS?

AMMONIUM MOLYBDATE INORGANIC PHOSPHORUS is a medical device that received FDA 510(k) clearance on 1980-10-10. The listed applicant is Panmed, Inc.. The 510(k) number is K802159.

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

AMMONIUM MOLYBDATE INORGANIC PHOSPHORUS received FDA 510(k) clearance on 1980-10-10, under 510(k) number K802159.

Who is the listed applicant for AMMONIUM MOLYBDATE INORGANIC PHOSPHORUS?

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

What is the FDA product code for AMMONIUM MOLYBDATE INORGANIC PHOSPHORUS?

The FDA product code for AMMONIUM MOLYBDATE INORGANIC PHOSPHORUS is CEO.

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Other records listing Panmed, 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.

K852767ERYTHOCYTE CREATINEK820642SICKLE-CHECKK8021648-HYDROXYQUINOLINE, CRESOLPHTHALEIN COM.K802157BCG REAGENT SERUM ALBUMIN W/TECHNICONK802163CHLORIDE COLOR & CHLORIDE SAMPLE DILUENTK802155REAGENTS SERUM SODIUM USING THE TECH.

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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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