Medical Device Recalls
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1 result found
510(K) Number: K142860 |
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Results per Page |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| Lumenis M22 System Model Number: GA-0005400 (M22 IPL + YAG Module) with Acne Filter (KT-1014971). | 2 | 05/13/2016 |
FEI # 3004135191 Lumenis Ltd |
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