K-number	K020055
Device name	PHILIPS INTEGRIS ALLURA 9 WITH FD OPTION
Applicant	Philips Medical Systems
Product code	JAA
Device class	Class II
Decision date	Mar 15, 2002
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 9 WITH FD OPTION

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