Carefusion 303, Inc. - FDA 510(k) Cleared Devices
Recent clearances: BD Alaris Infusion System with Guardrails Suite MX, BD Alaris System with Guardrails Suite MX v12.1.2
7
Total
7
Cleared
0
Denied
FDA 510(k) Regulatory Record - Carefusion 303, Inc. Cardiovascular ✕
2 devices