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FDA 510(k) Applications Submitted by VYGON S A
FDA 510(k) Number
Submission Date
Device Name
Applicant
K040657
03/12/2004
BOUSSIGNAC/VYGON ENDOTRACHEAL TUBE, MODEL 6501.25/30/35 AND 6502.70/75/80
VYGON S A
K013884
11/23/2001
BOUSSIGNAC C.P.A.P. DEVICE
VYGON S A
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