Medical Device Recalls
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1 result found
510(K) Number: K162054 |
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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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Single Chamber Temporary External Pacemaker, Model 53401 | 2 | 06/29/2018 | Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF) |
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