Medical Device Recalls
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1 result found
510(K) Number: K052582 |
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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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| DATEX-OHMEDA S/5 SINGLE-WIDTH AIRWAY MODULE, E-MINIC AND ACCESSORIES. DATEX-OHMEDA S/5TM FM WITH... | 1 | 07/18/2014 |
FEI # 2126677 GE Healthcare, LLC |
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