Medical Device Recalls
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1 result found
510(K) Number: K983591 |
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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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| Echosight Jansen-Anderson Intratubal Transfer Set, Catalog Number: K-J-JITS-572900, Global Product N... | 2 | 03/26/2018 | Cook Inc. |
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