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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: K921133
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BD BACTEC(TM) Standard 10 Aerobic/F Medium, catalog 442260, packed in tubes, 50 tubes/case and label... 3 03/08/2010 FEI # 1119779
Becton Dickinson & Co.
BD BACTEC(TM) Plus Anaerobic/F Medium, catalog 442193, packed in tubes, 50 tubes/case and labeled in... 3 03/08/2010 FEI # 1119779
Becton Dickinson & Co.
BD BACTEC(TM) Plus + Aerobic/F Medium, catalog 442192, packed in tubes, 50 tubes/case and labeled in... 3 03/08/2010 FEI # 1119779
Becton Dickinson & Co.
BD BACTEC(TM) Lytic 10 Anaerobic/F Medium, catalog 442265, packed in tubes, 50 tubes/case and labele... 3 03/08/2010 FEI # 1119779
Becton Dickinson & Co.
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