DERMA PRENE
K-Number: K820665 · 1982-05-03
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Device Summary
Frequently Asked Questions
What is the DERMA PRENE?
DERMA PRENE is a medical device that received FDA 510(k) clearance on 1982-05-03. The listed applicant is Ansell, Inc.. The 510(k) number is K820665.
When did DERMA PRENE receive FDA 510(k) clearance?
DERMA PRENE received FDA 510(k) clearance on 1982-05-03, under 510(k) number K820665.
Who is the listed applicant for DERMA PRENE?
The FDA 510(k) record lists Ansell, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for DERMA PRENE?
The FDA product code for DERMA PRENE is KGO.
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 Ansell, 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: KGO)
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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