Neostar Medical Technologies, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Neostar Medical Technologies, Inc. - FDA 510(k) Cleared Devices
4
Total
4
Cleared
0
Denied
Neostar Medical Technologies, Inc. has 4 FDA 510(k) cleared medical devices. Based in New Brunswick, US.
Historical record: 4 cleared submissions from 1995 to 1996. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Neostar Medical Technologies, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Neostar Medical Technologies, Inc.
4 devices
Cleared
Aug 08, 1996
SPREADABLE SHEATH INTRODUCER SET
Cardiovascular
177d
Cleared
Mar 13, 1995
DUAL LUMEN CATHETER (DLC) TRAY
Gastroenterology & Urology
333d
Cleared
Mar 13, 1995
ACUTE CENTRAL VENOUS ACCESS CATHETER (ACVAC)
General Hospital
179d
Cleared
Mar 13, 1995
ACUTE CENTRAL VENOUS ACCESS CATHETER TRAY
General Hospital
173d