MyoWorx TM20— 510(k) K192746
Substantially EquivalentMyoworx, Inc.
FDA 510(k) clearance K192746 for MyoWorx TM20, Substantially Equivalent on 2021-10-19. Applicant: Myoworx, Inc.. Device class: 2.
Clearance details
- Applicant
- Myoworx, Inc.
- Product code
- Code IPF
- Device class
- Class 2
- Regulation
- 21 CFR 890.5850
- Advisory panel
- Physical Medicine
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Guelph, CA
Recent devices under product code IPF
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