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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: K991362
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HYDRAGEL 15 Alkaline Hemoglobin (E) kit, in vitro diagnostic, Sebia Parc Technologique Leonard de Vi... 3 10/25/2006 FEI # 3001595416
Sebia, Inc.
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