Precision Vascular Systems, Inc. is one of 25810 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Precision Vascular Systems, Inc. - FDA 510(k) Cleared Devices
Recent clearances: PVS 1700 STEERABLE DELIVERY SYSTEM MICROCATHETER, PVS 1300 SYNCHRO 0.014 & PVS 1600 SYNCHRO 0.010 GUIDE WIRES, PVS 1600 SYNCHRO 0.010 NEURO GUIDE WIRE
7
Total
7
Cleared
0
Denied
Precision Vascular Systems, Inc. has 7 FDA 510(k) cleared medical devices. Based in Salt Lake City, US.
Historical record: 7 cleared submissions from 1999 to 2003. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Precision Vascular Systems, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Entela, Inc. as regulatory consultant.
FDA 510(k) Regulatory Record - Precision Vascular Systems, Inc.
7 devices
Cleared
Sep 05, 2003
PVS 1700 STEERABLE DELIVERY SYSTEM MICROCATHETER
Cardiovascular
23d
Cleared
Aug 12, 2003
PVS 1300 SYNCHRO 0.014 & PVS 1600 SYNCHRO 0.010 GUIDE WIRES
Cardiovascular
29d
Cleared
Dec 04, 2002
PVS 1600 SYNCHRO 0.010 NEURO GUIDE WIRE
Cardiovascular
30d
Cleared
Mar 21, 2002
PVS 1500 SDS
Cardiovascular
15d
Cleared
Mar 08, 2001
PVS 1300 NEURO GUIDE WIRE
Cardiovascular
171d
Cleared
Nov 08, 2000
PVS 1400 GUIDE WITE WITH HYDROPHILIC COATING
Cardiovascular
70d
Cleared
Jul 23, 1999
PVS 1400 GUIDEWIRE
Cardiovascular
133d