Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K140679 |
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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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365®M Lithotripsy Fiber- Reusable; Sure F!ex laser fibers are intended for use in laser-based sur... | 2 | 07/21/2015 | American Medical Systems Innovation Center - Silicon Valley |
200®M Lithotripsy Fiber- Reusable; Sure F!ex laser fibers are intended for use in laser-based sur... | 2 | 07/21/2015 | American Medical Systems Innovation Center - Silicon Valley |
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