Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K932553 |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| Capio CL; Model #M0068311350. Indicated for the placement of suture in a variety of Transvaginal ... | 2 | 05/04/2018 | Boston Scientific Corporation |
| Capio Standard Box 4 (Capio PC); Model #M0068312321. Intended for use in general suturing applica... | 2 | 05/04/2018 | Boston Scientific Corporation |
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