Cross Vascular, Inc.
FDA 510(k) & PMA Approved Devices — 2 products
Total Devices2
Categories2
Latest FDA decision2023-10-12
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K232852 | Cross Vascular RF Transseptal Needle, Cross Vascular Connection Cable | DXF | 2023-10-12 | View |
| 510(k) | K232809 | Cross Vascular RF Generator and Footswitch (optional accessory) | GEI | 2023-10-12 | View |
No matching devices.