FDA 510(k)

UCA GEL PRODUCT REFORMAULATION

K-Number: K802649 · 1980-11-12

Decision Date1980-11-12

Product CodeGYB

Advisory CommitteeNE

DecisionSubstantially Equivalent

Device Summary

UCA GEL PRODUCT REFORMAULATION 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 1980-11-12 under 510(k) number K802649. The device is classified under product code GYB. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the UCA GEL PRODUCT REFORMAULATION?

UCA GEL PRODUCT REFORMAULATION is a medical device that received FDA 510(k) clearance on 1980-11-12. The listed applicant is Vanaray Laboratories, Inc.. The 510(k) number is K802649.

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

UCA GEL PRODUCT REFORMAULATION received FDA 510(k) clearance on 1980-11-12, under 510(k) number K802649.

Who is the listed applicant for UCA GEL PRODUCT REFORMAULATION?

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 PRODUCT REFORMAULATION?

The FDA product code for UCA GEL PRODUCT REFORMAULATION is GYB.

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Other records listing Vanaray Laboratories, Inc. as applicant

K802647ECA GEL PROUDUCT REFORMULATION K802648UCA CREAM PRODUCT REFORMULATION K802650UCA LOTION PRODUCT REFORMULATION K801383ECA CREAM REFORMULATION K792490UCA LOTION K792489UCA CREAM

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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.