Medical Device Recalls
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1 result found
510(K) Number: K090808 |
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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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| Pinnacle Radiation Therapy Planning System: Multimodality Simulation Workspace 18.0.5 Model 87025... | 2 | 09/16/2025 | Philips Medical Systems (Cleveland) Inc |
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