K-number	K955484
Device name	XENON OPTION TO PRISM 3000
Applicant	Philips Medical Systems (Cleveland), Inc.
Product code	KPS
Device class	Class II
Decision date	Mar 29, 1996
Decision	Substantially Equivalent
Regulation	892.1200

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View the full FDA submission: accessdata.fda.gov

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XENON OPTION TO PRISM 3000

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