K-number	K120255
Device name	PHILIPS MICRODOSE
Applicant	Philips Digital Mammography Sweden AB
Product code	MUE
Device class	Class II
Decision date	Apr 19, 2012
Decision	Substantially Equivalent
Regulation	892.1715

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Source

View the full FDA submission: accessdata.fda.gov

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PHILIPS MICRODOSE

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