Medical Device Recalls
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1 result found
510(K) Number: K031810 |
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Results per Page |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| AMPLATZER Vascular Plug, Manufactured by AGA Medical Corporation , 682 Mendelssohn Avenue, Golden Va... | 3 | 11/05/2005 |
FEI # 3005334138 AGA Medical Corporation |
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