Medical Device Recalls
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1 result found
510(K) Number: K130195 |
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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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Array LaserLink, Manufactured by Lumenis, The Array" LaserLink" is a laser system accessory inten... | 2 | 09/30/2014 | Lumenis, Inc. |
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