Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K080753 |
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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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| DS Titanium Ligation Clip Appliers, used in laparoscopic surgery | 2 | 04/02/2018 | Aesculap Implant Systems LLC |
| DS Titanium Ligation Clip, used in laparoscopic surgery | 2 | 04/02/2018 | Aesculap Implant Systems LLC |
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