Medical Device Recalls
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1 result found
510(K) Number: K152181 |
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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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| 2.3mm Turbo-Power OTW, Manual, Model No 423-050 Product Usage The Turbo-Power System (Laser Atherec... | 2 | 02/05/2016 |
FEI # 3007284006 Spectranetics Corp. |
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