Vascular Technology Incorporated
FDA Regulatory Profile
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 11
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|
| K082870 | VTI INTRAOPERATIVE DOPPLER SYSTEMS | October 28, 2008 |
| K031091 | VTI 20 MHZ GATED DOPPLER | April 23, 2003 |
| K002990 | VTI ADULT DISPOSABLE SKULL PIN, MODEL 22000; VTI SKULL SCREW, MODEL 22001 | November 6, 2000 |
| K944764 | VTI DISPOSABLE PRESSURE DISPLAY SET | December 27, 1994 |
| K922738 | VTI OXYGEN ANALYZER | January 27, 1993 |
| K890058 | VASCULAR TECHNOLOGY UNIOX OXYGEN ALARM | November 21, 1989 |
| K883960 | GIPHY MONITOR | October 4, 1989 |
| K864583 | CARDIAC PERFORMANCE MONITOR | May 11, 1987 |
| K862114 | KHURI REGIONAL TISSUE PH MONITOR | June 25, 1986 |
| K862113 | NO. 100352 GALVANIC OXYGEN SENSOR | June 19, 1986 |
| K852275 | VASCULAR TECH # 100123 POLAROGRAPHIC OXGYEN SENSOR | June 20, 1985 |