PRODERMA LIQUID BANDAGE— 510(k) K063202

Name: FDA 510(k) clearance K063202
Creator: U.S. Food and Drug Administration
Published: 2007-05-02

Substantially Equivalent

Procurement Technology Systems, LLC

FDA 510(k) clearance K063202 for PRODERMA LIQUID BANDAGE, Substantially Equivalent on 2007-05-02. Applicant: Procurement Technology Systems, LLC. Device class: 1.

Clearance details

Applicant: Procurement Technology Systems, LLC
Product code: Code KMF
Device class: Class 1
Regulation: 21 CFR 880.5090
Advisory panel: General Hospital
Date received: 2006-10-20
Decision date: 2007-05-02
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Greer, SC, US

Download summary PDF View on FDA.gov ↗

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Data sourced from openFDA. This site is unofficial and independent of the FDA.