CER-S
Aug 2020
282d
Cardiocalm
1
Total
1
Cleared
0
Denied
Cardiocalm — FDA 510(k) Submissions
Cardiocalm has submitted 1 FDA 510(k) premarket notifications since 2020, of which 1 received clearance as substantially equivalent to a predicate device.
The company's most frequent device categories include Electrocardiograph, Ambulatory, With Analysis Algorithm . Use the specialty filter in the sidebar to narrow results.
1 devices