CONDUCT ALOE GEL, #UP239-8FL. OZ/#UP245 G-1 GALLON
K-Number: K925466 · 1993-08-26
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Device Summary
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
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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