ENDOPLUS hand-held laparoscopic instruments
Dec 2015
196d
Endoplus
1
Total
1
Cleared
0
Denied
Endoplus — FDA 510(k) Submissions
Endoplus 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 Coagulator, Culdoscopic (and Accessories) . Use the specialty filter in the sidebar to narrow results.
1 devices