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Neothermia Corp.

FDA 510(k) & PMA Approved Devices — 7 products

Total Devices7

Categories0

Latest FDA decision

Type	Number	Device Name	Code	Date	Actions
510(k)	K041347	MODIFICATION TO EN-BLOC BIOPSY SYSTEM	GEI	2004-06-04	View
510(k)	K033427	MODIFICATION TO EN-BLOC BIOPSY SYSTEM	KNW	2003-11-10	View
510(k)	K023413	MODIFICATION TO NEOTHERMIA'S EN-BLOC BIOPSY SYSTEM	GEI	2002-11-08	View
510(k)	K022296	MODIFICATION TO EN-BLOC BIOPSY SYSTEM	GEI	2002-07-30	View
510(k)	K021577	MODIFICATION TO EN-BLOC BIOPSY SYSTEM	GEI	2002-05-29	View
510(k)	K020031	EN-BLOC BIOPSY SYSTEM, MODELS 777-110, 777-120, 770-001, 777002, 777-006, 777-301, 777-302	GEI	2002-03-27	View
510(k)	K003190	EN BLOC BIOPSY SYSTEM	GEI	2001-06-11	View

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