WHOOP ECG (electrocardiogram) Feature (1.0)
Apr 2025
176d
Whoop., Inc.
1
Total
1
Cleared
0
Denied
Whoop., Inc. — FDA 510(k) Submissions
Whoop., Inc. has submitted 1 FDA 510(k) premarket notifications since 2025, of which 1 received clearance as substantially equivalent to a predicate device.
The company's most frequent device categories include Electrocardiograph Software For Over-the-counter Use . Use the specialty filter in the sidebar to narrow results.
1 devices