Neothermia Corp. is one of 15071 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Neothermia Corp. - FDA 510(k) Cleared Devices
Recent clearances: MODIFICATION TO EN-BLOC BIOPSY SYSTEM
7
Total
7
Cleared
0
Denied
Neothermia Corp. has 7 FDA 510(k) cleared medical devices. Based in Natick, US.
Historical record: 7 cleared submissions from 2001 to 2004. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Neothermia Corp. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Neothermia Corp.
7 devices
Cleared
Jun 04, 2004
MODIFICATION TO EN-BLOC BIOPSY SYSTEM
General & Plastic Surgery
15d
Cleared
Nov 10, 2003
MODIFICATION TO EN-BLOC BIOPSY SYSTEM
Gastroenterology & Urology
13d
Cleared
Nov 08, 2002
MODIFICATION TO NEOTHERMIA'S EN-BLOC BIOPSY SYSTEM
General & Plastic Surgery
28d
Cleared
Jul 30, 2002
MODIFICATION TO EN-BLOC BIOPSY SYSTEM
General & Plastic Surgery
14d
Cleared
May 29, 2002
MODIFICATION TO EN-BLOC BIOPSY SYSTEM
General & Plastic Surgery
15d
Cleared
Mar 27, 2002
EN-BLOC BIOPSY SYSTEM, MODELS 777-110, 777-120, 770-001, 777002, 777-006,...
General & Plastic Surgery
82d
Cleared
Jun 11, 2001
EN BLOC BIOPSY SYSTEM
General & Plastic Surgery
243d