CPR BAND
Mar 2021
268d
Credo
1
Total
1
Cleared
0
Denied
Credo — FDA 510(k) Submissions
Credo has submitted 1 FDA 510(k) premarket notifications since 2021, of which 1 received clearance as substantially equivalent to a predicate device.
The company's most frequent device categories include Aid, Cardiopulmonary Resuscitation . Use the specialty filter in the sidebar to narrow results.
1 devices