Medical Device Recalls
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1 result found
510(K) Number: K131473 |
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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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| Quanta System Sterile Optical Laser Fiber, single use | 2 | 06/10/2021 | Quanta System, S.p.A. |
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