Medical Device Recalls
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1 result found
510(K) Number: K112977 |
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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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Alcon Monarch III (1) "C" Cartridge The device is used for implanting AcrySof intraocular lenses in... | 2 | 01/09/2017 | Alcon Research, Ltd. |
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