Neothermia Corporation is one of 25353 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Neothermia Corporation - FDA 510(k) Cleared Devices
Recent clearances: MODIFICATION TO EN-BLOC BIOPSY SYSTEM, NEOTHERMIA EN-BLOC BIOPSY SYSTEM, EN-BLOC BIOPSY SYSTEM MODEL#777-110,777-001,777-002,777-006,777-301,777-302,777-115,777-120
3
Total
3
Cleared
0
Denied
Neothermia Corporation has 3 FDA 510(k) cleared medical devices. Based in Natick, US.
Historical record: 3 cleared submissions from 2004 to 2005. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Neothermia Corporation Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Neothermia Corporation
3 devices