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