COMPRESAID
Apr 1988
18d
R. Evans Corp.
1
Total
1
Cleared
0
Denied
R. Evans Corp. — FDA 510(k) Submissions
R. Evans Corp. has submitted 1 FDA 510(k) premarket notifications since 1988, of which 1 received clearance as substantially equivalent to a predicate device.
The company's most frequent device categories include Splint, Extremity, Inflatable, External . Use the specialty filter in the sidebar to narrow results.
1 devices