Medical Device Manufacturer · US , Fairfax , VA

Fitbit, Inc. - FDA 510(k) Cleared Devices

3 submissions · 3 cleared · Since 2014
3
Total
3
Cleared
0
Denied

Fitbit, Inc. has 3 FDA 510(k) cleared medical devices. Based in Fairfax, US.

Last cleared in 2022. Active since 2014. Primary specialty: Cardiovascular.

Browse the FDA 510(k) cleared devices submitted by Fitbit, Inc. Filter by specialty or product code using the sidebar.

FDA 510(k) cleared devices by Fitbit, Inc.

3 devices
1-3 of 3
Filters