Physiotrace
Aug 2017
117d
Nimbleheart, Inc.
1
Total
1
Cleared
0
Denied
Nimbleheart, Inc. — FDA 510(k) Submissions
Nimbleheart, Inc. has submitted 1 FDA 510(k) premarket notifications since 2017, of which 1 received clearance as substantially equivalent to a predicate device.
The company's most frequent device categories include Electrode, Electrocardiograph . Use the specialty filter in the sidebar to narrow results.
1 devices