K-number	K173408
Device name	Mammomat Revelation
Applicant	Siemens Medi Cal Solutions, Inc.
Product code	MUE
Device class	Class II
Decision date	Mar 21, 2018
Decision	Substantially Equivalent
Regulation	892.1715

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Source

View the full FDA submission: accessdata.fda.gov

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Mammomat Revelation

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