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

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

2 devices
1-2 of 2
Cleared Apr 08, 2022
Fitbit Irregular Rhythm Notifications
K212372 · QDB
Cardiovascular · 252d
Cleared Sep 11, 2020
Fitbit ECG App
K200948 · QDA
Cardiovascular · 156d
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All3 Cardiovascular 2 Gastroenterology & Urology 1