K-number	K023014
Device name	VIANOX DELIVERY SYSTEM, MODEL I
Applicant	Pulmonox Medical, Inc.
Product code	MRP
Device class	Class II
Decision date	Aug 14, 2003
Decision	Substantially Equivalent
Regulation	868.2380

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View the full FDA submission: accessdata.fda.gov

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VIANOX DELIVERY SYSTEM, MODEL I

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