PHYSICAL MONITORING REGISTRATION UNIT-S (PMRU-S)
Sep 2013
269d
Oktx, LLC
1
Total
1
Cleared
0
Denied
Oktx, LLC — FDA 510(k) Submissions
Oktx, LLC 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