VEIN-GOGH INSTRUMENT— 510(k) K112334

Substantially Equivalent

Refine USA, LLC

FDA 510(k) clearance K112334 for VEIN-GOGH INSTRUMENT, Substantially Equivalent on 2012-05-08. Applicant: Refine USA, LLC.

Clearance details

Applicant: Refine USA, LLC
Product code: Code ONQ
Advisory panel: General, Plastic Surgery
Date received: 2011-08-12
Decision date: 2012-05-08
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Jacksonville Beach, FL, US

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