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FDA 510(k)

INORGANIC PHOSPHORUS REAGENT

K-Number: K955937 · 1996-03-12

ApplicantDerma Media Lab., Inc.
Decision Date1996-03-12
Product CodeCEO
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

INORGANIC PHOSPHORUS REAGENT is the device name listed in this FDA 510(k) record. The listed applicant is Derma Media Lab., Inc.. It received FDA 510(k) clearance on 1996-03-12 under 510(k) number K955937. 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 REAGENT?

INORGANIC PHOSPHORUS REAGENT is a medical device that received FDA 510(k) clearance on 1996-03-12. The listed applicant is Derma Media Lab., Inc.. The 510(k) number is K955937.

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

INORGANIC PHOSPHORUS REAGENT received FDA 510(k) clearance on 1996-03-12, under 510(k) number K955937.

Who is the listed applicant for INORGANIC PHOSPHORUS REAGENT?

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

What is the FDA product code for INORGANIC PHOSPHORUS REAGENT?

The FDA product code for INORGANIC PHOSPHORUS REAGENT is CEO.

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Other records listing Derma Media Lab., 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.

K970664GLUCOSE REAGENTK971309UREAK971072CHOLESTEROL REAGENTK971005TRIGLYCERIDESK970867URIC ACID REAGENTK964915MAGNESIUM

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Related Devices (Code: CEO)

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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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