INJECTO FLUSH
Dec 1996
76d
Robert J. Jynch, Jr.
1
Total
1
Cleared
0
Denied
Robert J. Jynch, Jr. — FDA 510(k) Submissions
Robert J. Jynch, Jr. has submitted 1 FDA 510(k) premarket notifications since 1996, of which 1 received clearance as substantially equivalent to a predicate device.
The company's most frequent device categories include Forceps, Biopsy, Non-electric . Use the specialty filter in the sidebar to narrow results.
1 devices