Medical Device Recalls
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1 result found
510(K) Number: K072313 |
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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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AGA Medical Corporation, Amplatzer TorqVue Delivery System 45-degree. REF: 9-1TV10F45/80. Designe... | 2 | 03/11/2010 | AGA Medical Corporation |
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