VAX-D GENESIS SYSTEM (THERAPEUTIC TABLE)— 510(k) K053503

Name: FDA 510(k) clearance K053503
Creator: U.S. Food and Drug Administration
Published: 2005-12-28

Substantially Equivalent

Vax-D Medical Technologies USA, L.C.

FDA 510(k) clearance K053503 for VAX-D GENESIS SYSTEM (THERAPEUTIC TABLE), Substantially Equivalent on 2005-12-28. Applicant: Vax-D Medical Technologies USA, L.C.. Device class: 2.

Clearance details

Applicant: Vax-D Medical Technologies USA, L.C.
Product code: Code ITH
Device class: Class 2
Regulation: 21 CFR 890.5900
Advisory panel: Physical Medicine
Date received: 2005-12-16
Decision date: 2005-12-28
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Oldsmar, FL, US

Download summary PDF View on FDA.gov ↗

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