Method Mobility - FDA 510(k) Cleared Devices
1
Total
1
Cleared
0
Denied
Method Mobility has 1 FDA 510(k) cleared medical devices. Based in Fresno, US.
Last cleared in 2023. Active since 2023. Primary specialty: Physical Medicine.
Browse the FDA 510(k) cleared devices submitted by Method Mobility Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Third Party Review Group, LLC as regulatory consultant.
FDA 510(k) Regulatory Record - Method Mobility
1 devices