Medical Device Recalls
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1 result found
510(K) Number: K121611 |
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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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St. Jude Medical, AGA Medical corporation, AMPLATZER® TorqVue® FX Delivery System. Model #'s: 9-ITVF... | 1 | 02/11/2013 | St Jude Medical Inc |
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