K-number	K152989
Device name	Mammotome revolve Dual Vacuum Assist Biopsy System
Applicant	Devicor Medical Products, Inc.
Product code	KNW
Device class	Class II
Decision date	Feb 25, 2016
Decision	Substantially Equivalent
Regulation	876.1075

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Source

View the full FDA submission: accessdata.fda.gov

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Mammotome revolve Dual Vacuum Assist Biopsy System

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