Medical Device Recalls
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1 result found
510(K) Number: K081472 |
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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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SmartPort CT Port Access System, Catalog number CT80STPD, AngioDynamics Incorporated The SmartPor... | 2 | 09/01/2009 | Angiodynamics, INC |
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