Nexgen Medical Systems, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Nexgen Medical Systems, Inc. - FDA 510(k) Cleared Devices
4
Total
4
Cleared
0
Denied
Nexgen Medical Systems, Inc. has 4 FDA 510(k) cleared medical devices. Based in Reno, US.
Historical record: 4 cleared submissions from 2009 to 2011. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Nexgen Medical Systems, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Nexgen Medical Systems, Inc.
4 devices
Cleared
Nov 10, 2011
NEXGEN EXPANDABLE CATHETER
Cardiovascular
402d
Cleared
Oct 20, 2011
NEXGEN PERIPHERAL MECHANICAL RETRIEVAL DEVICE
Cardiovascular
260d
Cleared
Jan 18, 2011
NEXGEN PERIPHERAL GUIDE CATHETER
Cardiovascular
104d
Cleared
Sep 24, 2009
NEXGEN PERIPHERAL MECHANICAL RETRIEVAL DEVICE - 200CM, MODEL MRD-1000
Cardiovascular
175d