The Kendal Co. - FDA 510(k) Cleared Devices
Recent clearances: MARHUKAR TRIPLE LUMEN CATHETER, MODEL 12 FR, KENDALL ULTRAMER COUDE FOLEY CATHETER, MODEL 1416C, KENDALL CURITY COUDE FOLEY CATHETER TRAY, MODEL 6946C, MONOJECT INSULIN SYRINGE
63
Total
60
Cleared
0
Denied
FDA 510(k) Regulatory Record - The Kendal Co. Orthopedic ✕
1 devices