FDA 510(k)

ELVI CREATININ

K-Number: K792402 · 1979-12-07

Decision Date1979-12-07

Product CodeCGX

Advisory CommitteeCH

DecisionSubstantially Equivalent

Device Summary

ELVI CREATININ 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 K792402. The device is classified under product code CGX. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ELVI CREATININ?

ELVI CREATININ 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 K792402.

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

ELVI CREATININ received FDA 510(k) clearance on 1979-12-07, under 510(k) number K792402.

Who is the listed applicant for ELVI CREATININ?

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 CREATININ?

The FDA product code for ELVI CREATININ is CGX.

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Other records listing Volu Sol Medical Industries as applicant

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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.