Medical Device Recalls
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1 result found
510(K) Number: K034036 |
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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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| Marathon Flow Directed Micro Catheter, Model #105-5055. Product Usage: The Marathon Flow Directed... | 2 | 09/27/2012 |
FEI # 3004904811 Micro Therapeutics Inc, Dba Ev3 Neurovascular |
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