K-number	K082605
Device name	VPAP AUTO WITH HUMIDAIRE 3I
Applicant	Resmed, Ltd.
Product code	BZD
Device class	Class II
Decision date	Jan 13, 2009
Decision	Substantially Equivalent
Regulation	868.5905

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Source

View the full FDA submission: accessdata.fda.gov

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VPAP AUTO WITH HUMIDAIRE 3I

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