Neuravi, Ltd.
4 FDA 510(k) clearances · Manufacturer
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| Record | Firm | Date |
|---|---|---|
| EmboTrap II Revascularization Device, EMBOTRAP III Revascularization Device (K212908) | Neuravi, Ltd. | 2021-10-13 |
| EMBOTRAP III Revascularization Device (K211338) | Neuravi, Ltd. | 2021-07-30 |
| EMBOTRAP III Revascularization Device (K193063) | Neuravi, Ltd. | 2020-07-14 |
| EmboTrap ll Revascularization Device (K173452) | Neuravi, Ltd. | 2018-05-09 |
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