K-number	K163052
Device name	Brevera Biopsy System with Corlumina Imaging Technology
Applicant	Hologic, Inc.
Product code	KNW
Device class	Class II
Decision date	Mar 29, 2017
Decision	Substantially Equivalent
Regulation	876.1075

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Source

View the full FDA submission: accessdata.fda.gov

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Brevera Biopsy System with Corlumina Imaging Technology

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