Medical Device Recalls
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1 result found
510(K) Number: K192350 |
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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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| Non-ablative Fractional Laser Systems, Model: WFB-01 | 2 | 12/05/2024 |
FEI # 3014310779 WINGDERM ELECTRO-OPTICS LTD. |
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