Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K011703 |
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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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Boston Scientific SlimLine 200 Micron Holmium Fiber Delivery Device, Catalog No. 840-840, Sterile, M... | 2 | 04/09/2008 | Lumenis, Inc. |
Lumenis brand DuoTome SideLite® 550 Micron Delivery System; laser systems for ablating soft tissue. ... | 2 | 10/12/2006 | Lumenis Inc. |
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