Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K955882 |
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Results per Page |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| MediChoice® Multifunction Electrode Part Number: MC171 OH | 1 | 10/15/2014 |
FEI # 1282497 Covidien LLC |
| Covidien Kendall 1710H Multi-Function Defibrillation Electrodes Part Number: 40000006 | 1 | 10/15/2014 |
FEI # 1282497 Covidien LLC |
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