K-number	K111765
Device name	FULL CORE BIOPSY SYSTEM
Applicant	Promex Technologies, LLC
Product code	KNW
Device class	Class II
Decision date	Sep 6, 2011
Decision	Substantially Equivalent
Regulation	876.1075

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Source

View the full FDA submission: accessdata.fda.gov

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FULL CORE BIOPSY SYSTEM

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