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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: K001885
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ORTHO CLINICAL DIAGNOSTICS INC VITROS BUN (60/CR 5CR/PK) ORCLNL REAGENT. 2 05/27/2025 FEI # 3004386693
Mckesson Medical-Surgical Inc. Corporate Office
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