Medical Device Recalls
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1 result found
510(K) Number: K080202 |
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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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NanoKnife Irreversible Electroporation System. System consists of multiple components: Generator, fo... | 2 | 01/27/2012 | Angiodynamics Worldwide Headquarters |
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