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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: K924853
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4 glass vials per box. 2/4ml vials of Sample Diluting Solution & 2/2ml vials of Calibration Verifica... 3 10/03/2007 FEI # 3005529799
Tosoh Bioscience Inc
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