K-number	K973215
Device name	STEREOTACTIC NEEDLE CORE BIOPSY SYSTEM
Applicant	Laurus Medical Corp.
Product code	KNW
Device class	Class II
Decision date	Nov 6, 1997
Decision	Substantially Equivalent
Regulation	876.1075

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View the full FDA submission: accessdata.fda.gov

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STEREOTACTIC NEEDLE CORE BIOPSY SYSTEM

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