K-number	K142839
Device name	GenCut Core Biopsy System
Applicant	Covidien, LLC
Product code	EOQ
Device class	Class II
Decision date	Apr 29, 2015
Decision	Substantially Equivalent
Regulation	874.4680

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Source

View the full FDA submission: accessdata.fda.gov

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GenCut Core Biopsy System

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