Cross Vascular, Inc.
FDA 510(k) & PMA Approved Devices — 2 products
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Total Devices2
Categories0
Latest FDA decision
| 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.
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