Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K230881 |
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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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| Change Healthcare Cardiology Hemodynamics Software | 2 | 07/02/2025 |
FEI # 3003757840 CHANGE HEALTHCARE CANADA COMPANY |
| Change Healthcare Cardiology Hemodynamics software | 2 | 01/16/2025 |
FEI # 3394 A L I Technologies Ltd |
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