Medical Device Recalls
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1 result found
510(K) Number: K142684 |
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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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Medtronic, 10 Fr FlexCath Select Steerable Sheath 990065. The FlexCath Select Steerable Sheat... | 1 | 03/17/2015 | Medtronic Inc. Cardiac Rhythm Disease Management |
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