Neptec Design Group, Ltd. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Neptec Design Group, Ltd. - FDA 510(k) Cleared Devices
4
Total
4
Cleared
0
Denied
Neptec Design Group, Ltd. has 4 FDA 510(k) cleared medical devices. Based in Chapel Hill, US.
Historical record: 4 cleared submissions from 2001 to 2003. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Neptec Design Group, Ltd. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Neptec Design Group, Ltd.
4 devices
Cleared
May 29, 2003
CARECOMPANION PATIENT STATION & NURSE STATION
Cardiovascular
318d
Cleared
May 02, 2003
CARECOMPANION PATIENT STATION/CARECOMPANION PATIENT STATION
Cardiovascular
212d
Cleared
May 22, 2002
N2000 BASE STATION
Cardiovascular
90d
Cleared
Nov 14, 2001
N2000 BASE STATION, N2001 NURSE STATION
Cardiovascular
85d