K-number	K141979
Device name	ALLURA XPER FD SERIES / ALLURA XPER OR TABLE SERIES
Applicant	Philips Medical Systems Netherland BV
Product code	OWB
Device class	Class II
Decision date	Aug 19, 2014
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 FD SERIES / ALLURA XPER OR TABLE SERIES

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