Medical Device Recalls
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1 to 4 of 4 Results
510(K) Number: K904392 |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| MultiLab Series II 2CP & 2CP Express non-invasive vascular diagnostic device, Model Number 11996-000... | 2 | 03/01/2023 | Unetixs Vascular, Inc. |
| MultiLab Series II REVO non-invasive vascular diagnostic device, Model Number 12950-0000-01 | 2 | 03/01/2023 | Unetixs Vascular, Inc. |
| MultiLab Series II ROODRA non-invasive vascular diagnostic device, Model Number 11986-0000-01 | 2 | 03/01/2023 | Unetixs Vascular, Inc. |
| MultiLab Series II LHS TI & ERGO non-invasive vascular diagnostic device, Model Number 11949-0000-01 | 2 | 03/01/2023 | Unetixs Vascular, Inc. |
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