Medical Device Recalls
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1 result found
510(K) Number: K122461 |
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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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| IntellaMap Orion High Resolution Mapping Catheter; Material number: M004RC64S0; Catalog number RC64... | 2 | 12/10/2014 |
FEI # 3001236349 Boston Scientific Corp |
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