Medical Device Recalls
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1 result found
510(K) Number: K201320 |
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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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| Brand Name: Quantum Perfusion Centrifugal Blood Pump CP22 with Integrated Sensors Product Name: Pum... | 2 | 03/13/2025 |
FEI # 3006126428 Spectrum Medical Inc |
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