Vygon SA
FDA 510(k) & PMA Approved Devices — 2 products
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Total Devices2
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K040657 | BOUSSIGNAC/VYGON ENDOTRACHEAL TUBE, MODEL 6501.25/30/35 AND 6502.70/75/80 | BTR | 2004-06-10 | View |
| 510(k) | K013884 | BOUSSIGNAC C.P.A.P. DEVICE | BYE | 2003-01-21 | View |
No matching devices.
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