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Vygon SA

2 FDA 510(k) clearances · Manufacturer

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RecordFirmDate
BOUSSIGNAC/VYGON ENDOTRACHEAL TUBE, MODEL 6501.25/30/35 AND 6502.70/75/80 (K040657)Vygon SA2004-06-10
BOUSSIGNAC C.P.A.P. DEVICE (K013884)Vygon SA2003-01-21

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Every clearance here is in the API, with alerts when new ones post.