Medical Device Manufacturer · US , Temecula , CA

Vygon SA - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 2003
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
K040657 · BTR
Anesthesiology · 90d
Cleared Jan 21, 2003
BOUSSIGNAC C.P.A.P. DEVICE
K013884 · BYE
Anesthesiology · 424d
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