Draegerwerk AG & CO Kgaa - FDA 510(k) Cleared Devices
Recent clearances: Evita (V800), VentStar Resus heated (N) (MP17030), VentStar Helix dual heated (N) Plus (MP02650), VentStar Helix heated (N) Plus (MP02608)
8
Total
8
Cleared
0
Denied
FDA 510(k) Regulatory Record - Draegerwerk AG & CO Kgaa General Hospital ✕
1 devices