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FDA 510(k)

PRODERMA LIQUID BANDAGE

K-Number: K063202 · 2007-05-02

Decision Date2007-05-02
Product CodeKMF
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

PRODERMA LIQUID BANDAGE is the device name listed in this FDA 510(k) record. The listed applicant is Procurement Technology Systems, LLC. It received FDA 510(k) clearance on 2007-05-02 under 510(k) number K063202. The device is classified under product code KMF. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

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

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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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