Medical Device Recalls
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1 result found
510(K) Number: K130454 |
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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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LIFEPAK 20e DEFIBRILLATOR/MONITOR, 3201273 Product Usage: The LIFEPAK 20e defibrillator/monitor ... | 1 | 01/11/2018 | Physio-Control, Inc. |
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