Medical Device Recalls
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1 result found
510(K) Number: K923945 |
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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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The Gyrus ACMI Pleatman Sac Tissue Removal System facilitates removal of specimens while minimizing ... | 2 | 09/19/2010 | Gyrus Acmi, Incorporated |
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