THE NEEDLE CATCHER
Sep 2005
114d
E.D.Medical , Ltd.
1
Total
1
Cleared
0
Denied
E.D.Medical , Ltd. — FDA 510(k) Submissions
E.D.Medical , Ltd. has submitted 1 FDA 510(k) premarket notifications since 2005, of which 1 received clearance as substantially equivalent to a predicate device.
The company's most frequent device categories include Forceps . Use the specialty filter in the sidebar to narrow results.
1 devices