Medical Device Recalls
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1 result found
510(K) Number: K874813 |
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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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Distributed in USA: Product Number: 40-2894: Reinforced Wound Closure, Latex Free Sterile EO Rx, ... | 2 | 08/20/2013 | Aspen Surgical Products, Inc. |
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