Teleflexmedical, Inc. - FDA 510(k) Cleared Devices
Recent clearances: Rüsch Latex Gold Foley Catheter, Teleflex Rusch SoftSimplastic Foley Catheters, Sheridan Spiral-Flex Endotracheal Tubes
64
Total
61
Cleared
0
Denied
FDA 510(k) Regulatory Record - Teleflexmedical, Inc. General Hospital ✕
1 devices