MyoWorx TM20— 510(k) K192746

Substantially Equivalent

Myoworx, Inc.

FDA 510(k) clearance K192746 for MyoWorx TM20, Substantially Equivalent on 2021-10-19. Applicant: Myoworx, Inc..

Clearance details

Applicant: Myoworx, Inc.
Product code: Code IPF
Advisory panel: Physical Medicine
Date received: 2019-09-30
Decision date: 2021-10-19
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Guelph, CA

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