PRODERMA LIQUID BANDAGE
K-Number: K063202 · 2007-05-02
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Device Summary
Frequently Asked Questions
What is the PRODERMA LIQUID BANDAGE?
PRODERMA LIQUID BANDAGE is a medical device that received FDA 510(k) clearance on 2007-05-02. The listed applicant is Procurement Technology Systems, LLC. The 510(k) number is K063202.
When did PRODERMA LIQUID BANDAGE receive FDA 510(k) clearance?
PRODERMA LIQUID BANDAGE received FDA 510(k) clearance on 2007-05-02, under 510(k) number K063202.
Who is the listed applicant for PRODERMA LIQUID BANDAGE?
The FDA 510(k) record lists Procurement Technology Systems, LLC as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for PRODERMA LIQUID BANDAGE?
The FDA product code for PRODERMA LIQUID BANDAGE is KMF.
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.
Related Devices (Code: KMF)
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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