MYOVISION 3.0 WIREFREE SYSTEM
Aug 2013
269d
Precision Biometrics, Inc.
1
Total
1
Cleared
0
Denied
Precision Biometrics, Inc. — FDA 510(k) Submissions
Precision Biometrics, Inc. has submitted 1 FDA 510(k) premarket notifications since 2013, of which 1 received clearance as substantially equivalent to a predicate device.
The company's most frequent device categories include Electromyograph, Diagnostic . Use the specialty filter in the sidebar to narrow results.
1 devices