DRX3000— 510(k) K022602

Substantially Equivalent

Axiom Usa., Inc.

FDA 510(k) clearance K022602 for DRX3000, Substantially Equivalent on 2003-01-23. Applicant: Axiom Usa., Inc..

Clearance details

Applicant: Axiom Usa., Inc.
Product code: Code ITH
Advisory panel: Physical Medicine
Date received: 2002-08-06
Decision date: 2003-01-23
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Tampa, FL, US

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