Myoworx, Inc. - FDA 510(k) Cleared Devices
1
Total
1
Cleared
0
Denied
Myoworx, Inc. has 1 FDA 510(k) cleared medical devices. Based in Guelph, CA.
Last cleared in 2021. Active since 2021. Primary specialty: Physical Medicine.
Browse the FDA 510(k) cleared devices submitted by Myoworx, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) cleared devices by Myoworx, Inc.
1 devices