Medical Device Recalls
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1 result found
510(K) Number: K232291 |
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Results per Page |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| Essenz HLM (Heart-Lung Machine), REF: 49-00-10, with Software | 2 | 11/27/2024 | LivaNova Deutschland GmbH |
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