Medical Device Recalls
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1 to 3 of 3 Results
510(K) Number: K162935 |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| Horizon PSU Stim Interconnecting Cable - Product Usage: Horizon is indicated for the treatment of Ma... | 2 | 05/13/2020 | The Magstim Company Limited |
| Magstim Rapid Therapy System consisting of: Rapid Mainframe, Rapid Single Power Supply Unit , Rapid ... | 2 | 04/11/2018 | The Magstim Company Limited |
| Rapid2 PSU Stim Interconnecting Cable - Product Usage: indicated for the treatment of Major Depres... | 2 | 05/13/2020 | The Magstim Company Limited |
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