K-number	K053151
Device name	RUBICOR MAGIC BREAST BIOPSY DEVICE
Applicant	Rubicor Medical, Inc.
Product code	KNW
Device class	Class II
Decision date	Nov 18, 2005
Decision	Substantially Equivalent
Regulation	876.1075

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View the full FDA submission: accessdata.fda.gov

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RUBICOR MAGIC BREAST BIOPSY DEVICE

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