Unetixs Vascular, Inc.
4 FDA 510(k) clearances · Recalling firm
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| Record | Firm | Date |
|---|---|---|
| MultiLab Series II 2CP & 2CP Express non-invasive vascular diagnostic device, Model Number recall (Z-1193-2023) | Unetixs Vascular, Inc. | 2023-03-01 |
| MultiLab Series II LHS TI & ERGO non-invasive vascular diagnostic device, Model Number 119 recall (Z-1194-2023) | Unetixs Vascular, Inc. | 2023-03-01 |
| MultiLab Series II ROODRA non-invasive vascular diagnostic device, Model Number 11986-0000 recall (Z-1195-2023) | Unetixs Vascular, Inc. | 2023-03-01 |
| MultiLab Series II REVO non-invasive vascular diagnostic device, Model Number 12950-0000-0 recall (Z-1196-2023) | Unetixs Vascular, Inc. | 2023-03-01 |
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Every clearance here is in the API, with alerts when new ones post.