K-number	K010435
Device name	PHILIPS BV PULSERA/ENDURA
Applicant	Philips Medical Systems, Inc.
Product code	OWB
Device class	Class II
Decision date	Mar 12, 2001
Decision	Substantially Equivalent
Regulation	892.1650

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View the full FDA submission: accessdata.fda.gov

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PHILIPS BV PULSERA/ENDURA

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