Medical Device Recalls
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21 to 21 of 21 Results
510(K) Number: K031187 |
Results per Page |
Product Description
|
Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
|
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Automated External Defibrillator - HeartStart MRx Monitor/Defibrillator | 2 | 12/21/2017 | Philips Electronics North America Corporation |
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