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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: K081997
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XVIVO Perfusion AB (Part of Vitrolife), THAM Solution, 3.3 mmol/ml, 50 mL, REF 99019, Sterile, Use... 2 07/12/2011 FEI # 3003274090
Vitrolife, Inc.
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