Vygon SA is one of 25167 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Vygon SA - FDA 510(k) Cleared Devices
Recent clearances: BOUSSIGNAC/VYGON ENDOTRACHEAL TUBE, MODEL 6501.25/30/35 AND 6502.70/75/80, BOUSSIGNAC C.P.A.P. DEVICE
2
Total
2
Cleared
0
Denied
Vygon SA has 2 FDA 510(k) cleared medical devices. Based in Temecula, US.
Historical record: 2 cleared submissions from 2003 to 2004. Primary specialty: Anesthesiology.
Browse the FDA 510(k) cleared devices submitted by Vygon SA Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Vygon SA
2 devices