Agile Devices, Inc. - FDA 510(k) Cleared Devices
1
Total
1
Cleared
0
Denied
Agile Devices, Inc. has 1 FDA 510(k) cleared medical devices. Based in Wellesley, US.
Last cleared in 2022. Active since 2022. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Agile Devices, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Strategic Device Solutions, LLC as regulatory consultant.
FDA 510(k) Regulatory Record - Agile Devices, Inc.
1 devices