Vascular Products, Inc.
FDA Regulatory Profile
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 3
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|
| K913733 | STERILE CHEST TUBE | October 8, 1991 |
| K910840 | VASCULAR BIOPSY FORCEPS | July 15, 1991 |
| K823447 | IMPLANTABLE PACING LEAD, TINED #3262 & | December 3, 1982 |