REMY Medical Therapy Laser System
May 2019
128d
Footdocprenur, LLC
1
Total
1
Cleared
0
Denied
Footdocprenur, LLC — FDA 510(k) Submissions
Footdocprenur, LLC has submitted 1 FDA 510(k) premarket notifications since 2019, of which 1 received clearance as substantially equivalent to a predicate device.
The company's most frequent device categories include Lasers For Temporary Increase Of Clear Nail In Patients With Onychomycosis . Use the specialty filter in the sidebar to narrow results.
1 devices