Medical Device Recalls
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1 result found
510(K) Number: K050639 |
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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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The Lumenis VersaCut Tissue Morcellator Product Usage: is intended for use under direct or end... | 1 | 02/14/2013 | Lumenis Limited |
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