Medical Device Recalls
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1 result found
510(K) Number: K093663 |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| BARD® BrachySource® Iodine125 radioactive seeds consist of a welded titanium capsule containing the ... | 2 | 04/27/2018 | Bard Brachytherapy, Inc. |
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