Medical Monofilament Sensory Screening Toool
Jan 2015
82d
Medical Monofilament Manufacturing
1
Total
1
Cleared
0
Denied
Medical Monofilament Manufacturing — FDA 510(k) Submissions
Medical Monofilament Manufacturing has submitted 1 FDA 510(k) premarket notifications since 2015, of which 1 received clearance as substantially equivalent to a predicate device.
The company's most frequent device categories include Esthesiometer . Use the specialty filter in the sidebar to narrow results.
1 devices