K-number	K953910
Device name	PHILIPS BV 300 SERIES
Applicant	Philips Medical Systems North America, Inc.
Product code	OXO
Device class	Class II
Decision date	Oct 18, 1995
Decision	Substantially Equivalent
Regulation	892.1650

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View the full FDA submission: accessdata.fda.gov

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PHILIPS BV 300 SERIES

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