Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K172060 |
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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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Capio SLIM Box 5, Model #M0068318261; Intended for use in general suturing applications during o... | 2 | 05/04/2018 | Boston Scientific Corporation |
Capio SLIM Suture Capturing Device, Model #M0068318250. Intended for use in general suturing appl... | 2 | 05/04/2018 | Boston Scientific Corporation |
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