Medical Device Recalls
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1 result found
510(K) Number: K181817 |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| Medtronic Confida Expandable Sheath, REF CES122230. To provide a guide for catheters or devices int... | 1 | 05/27/2020 |
FEI # 3002806434 Medtronic Vascular Galway DBA Medtronic Ireland |
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