K-number	K050737
Device name	NEOTHERMIA EN-BLOC BIOPSY SYSTEM
Applicant	Neothermia Corporation
Product code	GEI
Device class	Class II
Decision date	Mar 31, 2005
Decision	Substantially Equivalent
Regulation	878.4400

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View the full FDA submission: accessdata.fda.gov

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NEOTHERMIA EN-BLOC BIOPSY SYSTEM

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