K-number	K102005
Device name	ALLURA XPER OR TABLE SERIES
Applicant	Philips Medical Systems North America, Inc.
Product code	OWB
Device class	Class II
Decision date	Aug 9, 2010
Decision	Substantially Equivalent
Regulation	892.1650

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Source

View the full FDA submission: accessdata.fda.gov

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ALLURA XPER OR TABLE SERIES

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