Medical Device Recalls
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1 result found
510(K) Number: K162001 |
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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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MR Coils The MR Coil is intended to be used in conjunction with a Magnetic Resonance Scanner to p... | 3 | 10/20/2020 | Invivo Corporation |
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