K-number	K091947
Device name	S8 ASPEN WITH H4I PLUS
Applicant	Resmed, Ltd.
Product code	BZD
Device class	Class II
Decision date	Sep 28, 2009
Decision	Substantially Equivalent
Regulation	868.5905

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View the full FDA submission: accessdata.fda.gov

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S8 ASPEN WITH H4I PLUS

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