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FDA 510(k)

ELVI INORGANIC PHOSPHOROUS

K-Number: K792401 · 1979-12-07

ApplicantVolu Sol Medical Industries
Decision Date1979-12-07
Product CodeCEO
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

ELVI INORGANIC PHOSPHOROUS is the device name listed in this FDA 510(k) record. The listed applicant is Volu Sol Medical Industries. It received FDA 510(k) clearance on 1979-12-07 under 510(k) number K792401. 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 ELVI INORGANIC PHOSPHOROUS?

ELVI INORGANIC PHOSPHOROUS is a medical device that received FDA 510(k) clearance on 1979-12-07. The listed applicant is Volu Sol Medical Industries. The 510(k) number is K792401.

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

ELVI INORGANIC PHOSPHOROUS received FDA 510(k) clearance on 1979-12-07, under 510(k) number K792401.

Who is the listed applicant for ELVI INORGANIC PHOSPHOROUS?

The FDA 510(k) record lists Volu Sol Medical Industries as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ELVI INORGANIC PHOSPHOROUS?

The FDA product code for ELVI INORGANIC PHOSPHOROUS is CEO.

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Other records listing Volu Sol Medical Industries 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.

K822128VOLU-SOL SINGLE DIFFERENTIAL STAINK822127VOLU-SOL ZENKERS FIXATIVEK822126VOLU-SOL CARNOY FLUIDK822129VOLU-SOL BOVINS FIXATIVEK822036VOLU-SOL DECALCIFERK822035VOLU-SOL GILLS EA

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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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