Medical Device Manufacturer · US , Temecula , CA

Vygon SA - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 2003

Recent clearances: BOUSSIGNAC/VYGON ENDOTRACHEAL TUBE, MODEL 6501.25/30/35 AND 6502.70/75/80, BOUSSIGNAC C.P.A.P. DEVICE

View 2 510(k) Devices ↓

2

Total

2

Cleared

0

Denied

FDA 510(k) Regulatory Record - Vygon SA Anesthesiology ✕

2 devices

1-2 of 2

Cleared Jun 10, 2004

BOUSSIGNAC/VYGON ENDOTRACHEAL TUBE, MODEL 6501.25/30/35 AND 6502.70/75/80

Anesthesiology · 90d

Cleared Jan 21, 2003

BOUSSIGNAC C.P.A.P. DEVICE

Anesthesiology · 424d