Nuvascular, Inc.
2 FDA 510(k) clearances · Manufacturer
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| Record | Firm | Date |
|---|---|---|
| HARBOR Occlusion Device (K260635) | Nuvascular, Inc. | 2026-06-12 |
| HARBOR Occlusion Device (K250133) | Nuvascular, Inc. | 2025-07-09 |
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