Mespere Lifesciences, Inc. - FDA 510(k) Cleared Devices
Recent clearances: VO200 – NeurOs Cerebral Oximetry System, Central Venous Pressure System, CENTRAL VENOUS PRESSURE SYSTEM - MESPERE VENUS 1000
3
Total
3
Cleared
0
Denied
FDA 510(k) Regulatory Record - Mespere Lifesciences, Inc. General & Plastic Surgery ✕
1 devices