Medical Device Recalls
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1 result found
510(K) Number: K140670 |
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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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| Ellipse ND: YAG Laser applicator for Ellipse Multiflex Medical Laser Products. | 2 | 06/09/2016 |
FEI # 3005112495 Ellipse A/S |
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