K-number	K023413
Device name	MODIFICATION TO NEOTHERMIA'S EN-BLOC BIOPSY SYSTEM
Applicant	Neothermia Corp.
Product code	GEI
Device class	Class II
Decision date	Nov 8, 2002
Decision	Substantially Equivalent
Regulation	—

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View the full FDA submission: accessdata.fda.gov

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MODIFICATION TO NEOTHERMIA'S EN-BLOC BIOPSY SYSTEM

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