K-number	K100011
Device name	FISHER & PAYKEL HEALTHCARE BUBBLE CPAP SYSTEM
Applicant	Fisher & Paykel Healthcare, Ltd.
Product code	BZD
Device class	Class II
Decision date	Oct 8, 2010
Decision	Substantially Equivalent
Regulation	868.5905

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View the full FDA submission: accessdata.fda.gov

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FISHER & PAYKEL HEALTHCARE BUBBLE CPAP SYSTEM

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