K-number	K921101
Device name	PHILIPS INTEGRIS V3000 FILM
Applicant	Philips Medical Systems, Inc.
Product code	IZI
Device class	Class II
Decision date	May 15, 1992
Decision	Substantially Equivalent
Regulation	892.1600

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View the full FDA submission: accessdata.fda.gov

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PHILIPS INTEGRIS V3000 FILM

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