AXXENT ELECTRONIC BRACHYTHERAPY SYSTEM— 510(k) K072683

Unknown

Xoft, Inc.

FDA 510(k) clearance K072683 for AXXENT ELECTRONIC BRACHYTHERAPY SYSTEM, Unknown on 2008-02-29. Applicant: Xoft, Inc..

Clearance details

Applicant: Xoft, Inc.
Product code: Code JAD
Advisory panel: Radiology
Date received: 2007-09-21
Decision date: 2008-02-29
Decision: Unknown
Clearance type: Traditional
Location: Fremont, CA, US

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