Vantis 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) | K262817 | CrossFAST Integrated Microcatheter Advanced Delivery System | DQY | 2026-09-18 | View |
| 510(k) | K242276 | CrossFAST™ Integrated Microcatheter Guide Extension System (CFM55) | DQY | 2024-09-30 | View |
No matching devices.
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