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FDA 510(k)

ELVI CHLORIDE

K-Number: K792400 · 1979-12-07

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

Device Summary

ELVI CHLORIDE 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 K792400. The device is classified under product code CHJ. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ELVI CHLORIDE?

ELVI CHLORIDE 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 K792400.

When did ELVI CHLORIDE receive FDA 510(k) clearance?

ELVI CHLORIDE received FDA 510(k) clearance on 1979-12-07, under 510(k) number K792400.

Who is the listed applicant for ELVI CHLORIDE?

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 CHLORIDE?

The FDA product code for ELVI CHLORIDE is CHJ.

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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: CHJ)

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.

K010670PICCOLO CHLORIDE TEST SYSTEMAbaxis, Inc.K945408340-CHLORIDE FOR DISCRETE RANDOM ACCESS ANALYZERCatachem, Inc.K943006CHLORIDE QVETPrisma SystemsK934136OLYMPUS CHLORIDE REAGENT, MODIFICATIONOlympus Corp.K932528OLYMPUS CHLORID REAGENT, MODIFIEDOlympus Corp.K925338OLYMPUS CHLORIDE REAGENTOlympus Corp.

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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