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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: K000762
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BD BBL Sensi Disc Moxifloxacin- 5 ug, used for semi-quantitative in vitro susceptibility testing. Ca... 2 02/08/2024 FEI # 1119779
Becton Dickinson & Co.
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