Medical Device Recalls
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1 result found
510(K) Number: K011670 |
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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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Datex-Ohmeda S/5 Oxygen Saturation Module (M-OSAT) | 2 | 03/05/2003 | Datex-Ohmeda |
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