Medical Device Recalls
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1 result found
510(K) Number: K202114 |
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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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| CoolSeal Generator, REF: CSL-200-50 | 2 | 03/08/2022 |
FEI # 3010377594 Bolder Surgical, LLC |
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