K-number	K040366
Device name	PRESSURE MANIFOLD, MODEL BC 110
Applicant	Fisher & Paykel Healthcare, Ltd.
Product code	CBP
Device class	Class II
Decision date	Mar 4, 2004
Decision	Substantially Equivalent
Regulation	868.5870

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View the full FDA submission: accessdata.fda.gov

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PRESSURE MANIFOLD, MODEL BC 110

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