Skydance Vascular, 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 |
|---|
| K250292 | OSPREY Midline Closed IV Catheter System (OspreyEDC-F20) | May 2, 2025 |
| K231626 | OSPREY Closed IV Catheter System (OspreyV2) | August 31, 2023 |
| K223018 | OSPREY PERIPHERAL IV Catheter System | April 14, 2023 |