Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K090233 |
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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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GE Datex-Ohmeda Aisys Anesthesia System, manufactured by GE Healthcare, P.O. Box 900, FIN-00031 GE, ... | 2 | 10/06/2010 | GE Healthcare, LLC |
GE, 1011-9000-000 Aisys Anesthesia Machine and Monitor | 1 | 05/11/2010 | Ge Healthcare, Llc |
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