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U.S. Department of Health and Human Services

Medical Device Recalls
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1 result found
510(K) Number: K070421
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Datex-Ohmeda S/5 Device Interfacing Solution, N-DISVENT 02. The Datex-Ohmeda S/5 Device Interfaci... 2 09/04/2009 FEI # 2126677
GE Medical Systems, LLC
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