Medical Device Recalls
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1 result found
510(K) Number: K883743 |
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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 Medical Device Identification Card for SureScan pacemaker patients. The front of ... | 2 | 10/05/2015 | Medtronic Inc. Cardiac Rhythm Disease Management |
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