Medical Device Recalls
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1 result found
510(K) Number: K100415 |
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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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| FemTouch delivery system includes the FemTouch Kit (AC-1007415) and FemTouch" Tip (SPSA-20002590) ... | 2 | 10/23/2016 |
FEI # 3004135191 Lumenis Limited |
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