Medical Device Recalls
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1 result found
510(K) Number: K111899 |
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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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Armada 35/ Armada 35 LL PTA Catheters. The device is intended for dilatation of lesions in the vascu... | 2 | 09/25/2012 | Abbott Vascular |
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