K-number	K083740
Device name	MAMMODIAGNOST VU
Applicant	Philips Medical Systems Nederland B.V.
Product code	LLZ
Device class	Class II
Decision date	Feb 13, 2009
Decision	Substantially Equivalent
Regulation	892.2050

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Source

View the full FDA submission: accessdata.fda.gov

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MAMMODIAGNOST VU

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