Medical Device Recalls
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1 result found
510(K) Number: K103386 |
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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, Launcher Guiding Catheter, Model # LA8EBU45SH, Lot # 0006722866, 8F and Model # LA6IMAD,... | 2 | 06/21/2013 | Medtronic Inc. Cardiac Rhythm Disease Management |
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