Medical Device Recalls
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1 result found
510(K) Number: K904039 |
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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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| Covidien Nellcor SpO2 Forehead Sensor Item Code: RS10; The Covidien Nellcor® Forehead SpO2Sensor... | 2 | 02/02/2017 |
FEI # 1219930 Covidien LLC |
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