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U.S. Department of Health and Human Services

Medical Device Recalls
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1 to 4 of 4 Results
510(K) Number: K844407
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BD DifcoTM Neisseria Meningitidis Antisera Group Y, 228811, 1mL, in vials, which were labeled in pa... 3 08/08/2008 FEI # 1025402
BD Diagnostic Systems / Lee Laboratories
BD DifcoTM Neisseria Meningitidis Antiserum Group Y 241113, 1mL, in vials, which were labeled in par... 3 08/08/2008 FEI # 1025402
BD Diagnostic Systems / Lee Laboratories
BD DifcoTM Neisseria Meningitidis Antisera Group Y 241113, 1mL, in vials, which were labeled in part... 3 08/08/2008 FEI # 1025402
BD Diagnostic Systems / Lee Laboratories
BD DifcoTM Neisseria Meningitidis Antisera Group Y 228811, 1mL, in vials, which were labeled in part... 3 08/08/2008 FEI # 1025402
BD Diagnostic Systems / Lee Laboratories
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