Nevap, Inc. - FDA 510(k) Cleared Devices
Recent clearances: NeVap Aspire Subglottic Suction Endotracheal Tube (ASSET) with Preloaded Stylet
1
Total
1
Cleared
0
Denied
FDA 510(k) Regulatory Record - Nevap, Inc. Anesthesiology ✕
1 devices