DRX 2000— 510(k) K010292

Substantially Equivalent

Axiom Worldwide, Inc.

FDA 510(k) clearance K010292 for DRX 2000, Substantially Equivalent on 2001-05-01. Applicant: Axiom Worldwide, Inc.. Device class: 2.

Clearance details

Applicant: Axiom Worldwide, Inc.
Product code: Code ITH
Device class: Class 2
Regulation: 21 CFR 890.5900
Advisory panel: Physical Medicine
Date received: 2001-01-31
Decision date: 2001-05-01
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Tampa, FL, 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.