K-number	K102771
Device name	BIOPSY HANDY, MRI BIOPSY HANDY
Applicant	Somatex Medical Technologies GmbH
Product code	KNW
Device class	Class II
Decision date	Jun 24, 2011
Decision	Substantially Equivalent
Regulation	876.1075

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View the full FDA submission: accessdata.fda.gov

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BIOPSY HANDY, MRI BIOPSY HANDY

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