Medical Device Recalls
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1 result found
510(K) Number: K072332 |
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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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Vari Lase WireFiber Laser Fiber, RED 7137, Rx ONLY, Sterile EO, Vascular Solutions Inc., 6464 Sycam... | 2 | 03/03/2011 | Vascular Solutions, Inc. |
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