K-number	K960317
Device name	LAURUS NEEDLE CORE BIOPSY SYSTEM
Applicant	Laurus Medical Corp.
Product code	FCG
Device class	Class II
Decision date	Mar 15, 1996
Decision	Substantially Equivalent
Regulation	876.1075

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View the full FDA submission: accessdata.fda.gov

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LAURUS NEEDLE CORE BIOPSY SYSTEM

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