Precision Vascular Systems, Inc.
FDA Regulatory Profile
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 7
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
| K032494 | PVS 1700 STEERABLE DELIVERY SYSTEM MICROCATHETER | September 5, 2003 |
| K032146 | PVS 1300 SYNCHRO 0.014 & PVS 1600 SYNCHRO 0.010 GUIDE WIRES | August 12, 2003 |
| K023700 | PVS 1600 SYNCHRO 0.010 NEURO GUIDE WIRE | December 4, 2002 |
| K020733 | PVS 1500 SDS | March 21, 2002 |
| K002907 | PVS 1300 NEURO GUIDE WIRE | March 8, 2001 |
| K002707 | PVS 1400 GUIDE WITE WITH HYDROPHILIC COATING | November 8, 2000 |
| K990823 | PVS 1400 GUIDEWIRE | July 23, 1999 |