KINESIA— 510(k) K063872

Substantially Equivalent

Cleveland Medical Devices, Inc.

FDA 510(k) clearance K063872 for KINESIA, Substantially Equivalent on 2007-04-06. Applicant: Cleveland Medical Devices, Inc..

Clearance details

Applicant: Cleveland Medical Devices, Inc.
Product code: Code GYD
Advisory panel: Neurology
Date received: 2006-12-29
Decision date: 2007-04-06
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Cleveland, OH, US

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