Medical Device Recalls
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1 result found
510(K) Number: K082786 |
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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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| PEAK brand PlasmaBlade EXT, Tissue Dissection Device, Catalogue Number: PS215-040; Product is ma... | 2 | 02/02/2011 |
FEI # 3007069406 Peak Surgical |
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