K-number	K013884
Device name	BOUSSIGNAC C.P.A.P. DEVICE
Applicant	Vygon SA
Product code	BYE
Device class	Class II
Decision date	Jan 21, 2003
Decision	Substantially Equivalent
Regulation	868.5965

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View the full FDA submission: accessdata.fda.gov

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BOUSSIGNAC C.P.A.P. DEVICE

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