Spiggle & Theis Medizintechnik GmbH - FDA 510(k) Cleared Devices
Recent clearances: TubaVent Balloon Dilatation System
1
Total
1
Cleared
0
Denied
FDA 510(k) Regulatory Record - Spiggle & Theis Medizintechnik GmbH Ear, Nose, Throat ✕
1 devices