VENX REVOLUTION— 510(k) K110355

Substantially Equivalent

Venx, LLC

FDA 510(k) clearance K110355 for VENX REVOLUTION, Substantially Equivalent on 2011-04-22. Applicant: Venx, LLC. Device class: 1.

Clearance details

Applicant: Venx, LLC
Product code: Code GAH
Device class: Class 1
Regulation: 21 CFR 878.4800
Advisory panel: General, Plastic Surgery
Date received: 2011-02-07
Decision date: 2011-04-22
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Tucson, AZ, 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.