K-number	K002016
Device name	PHILIPS INTEGRIS ALLURA
Applicant	Philips Medical Systems North America, Inc.
Product code	OWB
Device class	Class II
Decision date	Sep 6, 2000
Decision	Substantially Equivalent
Regulation	892.1650

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View the full FDA submission: accessdata.fda.gov

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PHILIPS INTEGRIS ALLURA

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