Neuravi Limited
3 FDA 510(k) clearances · Manufacturer
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| Record | Firm | Date |
|---|---|---|
| EMBOTRAP III Revascularization Device (K251789) | Neuravi Limited | 2025-09-25 |
| EMBOGUARD Balloon Guide Catheter (K233924) | Neuravi Limited | 2024-04-18 |
| EMBOGUARD Balloon Guide Catheter (K212340) | Neuravi Limited | 2021-12-17 |
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Every clearance here is in the API, with alerts when new ones post.