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FDA 510(k)

CONDUCT ALOE GEL, #UP239-8FL. OZ/#UP245 G-1 GALLON

K-Number: K925466 · 1993-08-26

Decision Date1993-08-26
Product CodeGYB
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

CONDUCT ALOE GEL, #UP239-8FL. OZ/#UP245 G-1 GALLON is the device name listed in this FDA 510(k) record. The listed applicant is Uni-Patch, Inc.. It received FDA 510(k) clearance on 1993-08-26 under 510(k) number K925466. 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 CONDUCT ALOE GEL, #UP239-8FL. OZ/#UP245 G-1 GALLON?

CONDUCT ALOE GEL, #UP239-8FL. OZ/#UP245 G-1 GALLON is a medical device that received FDA 510(k) clearance on 1993-08-26. The listed applicant is Uni-Patch, Inc.. The 510(k) number is K925466.

When did CONDUCT ALOE GEL, #UP239-8FL. OZ/#UP245 G-1 GALLON receive FDA 510(k) clearance?

CONDUCT ALOE GEL, #UP239-8FL. OZ/#UP245 G-1 GALLON received FDA 510(k) clearance on 1993-08-26, under 510(k) number K925466.

Who is the listed applicant for CONDUCT ALOE GEL, #UP239-8FL. OZ/#UP245 G-1 GALLON?

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

What is the FDA product code for CONDUCT ALOE GEL, #UP239-8FL. OZ/#UP245 G-1 GALLON?

The FDA product code for CONDUCT ALOE GEL, #UP239-8FL. OZ/#UP245 G-1 GALLON is GYB.

Related Clinical Trials

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.

Other records listing Uni-Patch, 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.

Related Devices (Code: GYB)

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.

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.

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