Medical Device Recalls
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1 result found
510(K) Number: K013013 |
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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 Select 3D Arterial Cannulae. Vented, model 78622 (22 Fr.). Non-Vented Cannulae, model 7... | 2 | 02/20/2014 | Medtronic Inc. Cardiac Rhythm Disease Management |
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