VAX-D GENESIS G2 SYSTEM— 510(k) K071347

Name: FDA 510(k) clearance K071347
Creator: U.S. Food and Drug Administration
Published: 2007-10-05

Substantially Equivalent

Vax-D Medical Technologies, LLC

FDA 510(k) clearance K071347 for VAX-D GENESIS G2 SYSTEM, Substantially Equivalent on 2007-10-05. Applicant: Vax-D Medical Technologies, LLC. Device class: 2.

Clearance details

Applicant: Vax-D Medical Technologies, LLC
Product code: Code ITH
Device class: Class 2
Regulation: 21 CFR 890.5900
Advisory panel: Physical Medicine
Date received: 2007-05-14
Decision date: 2007-10-05
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Oldsmar, FL, US

Download summary PDF View on FDA.gov ↗

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