Rusch SoftSimplastic Foley Catheters
Jan 2026
161d
Teleflex Medical Sdn. Bhd.
1
Total
1
Cleared
0
Denied
Teleflex Medical Sdn. Bhd. — FDA 510(k) Submissions
Teleflex Medical Sdn. Bhd. has submitted 1 FDA 510(k) premarket notifications since 2026, of which 1 received clearance as substantially equivalent to a predicate device.
The company's most frequent device categories include Catheter, Retention Type, Balloon . Use the specialty filter in the sidebar to narrow results.
1 devices