Medical Device Recalls
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1 result found
510(K) Number: K121767 |
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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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Cardioblate" Gemini"-s Irrigated RF Surgical Ablation System; The device is placed in a plastic tray... | 2 | 05/25/2022 | Medtronic Perfusion Systems |
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