Medical Device Recalls
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1 result found
510(K) Number: K011135 |
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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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GSI Audera (version 2.6 software) Viasys Healthcare, Inc. Part or (Catalog) Numbers: 2001-9700, 2... | 2 | 11/12/2008 | Cardinal Health, Inc |
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