Terumo America, Inc. - FDA 510(k) Cleared Devices
Recent clearances: PLASMA FLEX, TERUMO HOLLOW FIBER OXYGENATOR, CLIRANS TH13 HOLLOW FIBER DIALYZER
31
Total
31
Cleared
0
Denied
FDA 510(k) Regulatory Record - Terumo America, Inc. General & Plastic Surgery ✕
1 devices