Medical Device Recalls
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1 result found
510(K) Number: K133272 |
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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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Lumenis VersaCut+ Tissue Morcellator GA-0007500 The Lumenis VersaCut / VersaCut+ Tissue Morcellat... | 2 | 09/16/2015 | Lumenis |
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