Medical Device Recalls
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1 result found
510(K) Number: K024118 |
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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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UltraFlow HPC Flow Directed Micro Catheter, Model # 105-5065. Product Usage: The UltraFlow HPC F... | 2 | 09/27/2012 | Micro Therapeutics Inc, Dba Ev3 Neurovascular |
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