FDA 510(k)

UCA GEL

K-Number: K792492 · 1980-02-05

Decision Date1980-02-05

Product CodeIYO

Advisory CommitteeRA

DecisionSubstantially Equivalent

Device Summary

UCA GEL is the device name listed in this FDA 510(k) record. The listed applicant is Vanaray Laboratories, Inc.. It received FDA 510(k) clearance on 1980-02-05 under 510(k) number K792492. The device is classified under product code IYO. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the UCA GEL?

UCA GEL is a medical device that received FDA 510(k) clearance on 1980-02-05. The listed applicant is Vanaray Laboratories, Inc.. The 510(k) number is K792492.

When did UCA GEL receive FDA 510(k) clearance?

UCA GEL received FDA 510(k) clearance on 1980-02-05, under 510(k) number K792492.

Who is the listed applicant for UCA GEL?

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

What is the FDA product code for UCA GEL?

The FDA product code for UCA GEL is IYO.

Other records listing Vanaray Laboratories, 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.

K802647ECA GEL PROUDUCT REFORMULATION K802648UCA CREAM PRODUCT REFORMULATION K802650UCA LOTION PRODUCT REFORMULATION K802649UCA GEL PRODUCT REFORMAULATION K801383ECA CREAM REFORMULATION K792490UCA LOTION

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.