Medical Device Recalls
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1 result found
510(K) Number: K012837 |
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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 Cardiocap/5 Anesthesia Monitor with N-XOSAT SpO2 measurement option | 2 | 03/05/2003 |
FEI # 2183066 Datex-Ohmeda |
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