Medical Device Recalls
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1 to 4 of 4 Results
510(K) Number: K191946 |
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Results per Page |
Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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Penumbra JET 7 Reperfusion Catheter REF 5MAXJET7 The Penumbra JET 7 Reperfusion Catheter with Xtr... | 1 | 01/18/2021 | Penumbra Inc. |
Penumbra JET 7MAX KIT Penumbra JET 7 Reperfusion Catheter+ MAX Delivery Device + Hi-Flow Aspiration ... | 1 | 01/18/2021 | Penumbra Inc. |
Penumbra JET 7 KIT Reperfusion Catheter+Penumbra Hi-Flow Aspiration Tubing REF 5MAXJET7L138KIT T... | 1 | 01/18/2021 | Penumbra Inc. |
Penumbra JET 7 KIT Reperfusion Catheter+Penumbra Hi-Flow Aspiration Tubing REF 5MAXJET7KIT The P... | 1 | 01/18/2021 | Penumbra Inc. |
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