Medical Device Recalls
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1 result found
510(K) Number: K213925 |
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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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| Power electronic box, Part #AS-0066, subassembly for the MyoCycle MC-2. | 2 | 08/16/2022 | Myolyn Inc. |
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