STERIS Corporation - FDA 510(k) Cleared Devices
Recent clearances: SYSTEM 1E Liquid Chemical Sterilant Processing System, Model P6700, Celerity 5 HP Biological Indicator (LCB052), Celerity™ 20 HP Biological Indicator
204
Total
202
Cleared
2
Denied
FDA 510(k) Regulatory Record - STERIS Corporation Cardiovascular ✕
1 devices