FDA 510(k) Applications Submitted by Becton, Dickinson and Company

FDA 510(k) Number Submission Date Device Name Applicant
K223286 10/25/2022 BD AutoShield DuoÖ Pen Needle Becton, Dickinson and Company
K222559 08/24/2022 BD BACTECÖ Myco/F Lytic Culture Vials Becton, Dickinson and Company
K220212 01/26/2022 BD Vacutainer« Push Button Blood Collection Set, BD Vacutainer« Push Button Blood Collection Set with Pre-Attached Holder Becton, Dickinson and Company
K193190 11/19/2019 BD PureHub Disinfecting Cap Becton, Dickinson and Company
K213955 12/17/2021 0.9% Sodium Chloride Injection, USP, BD PosiFlush SafeScrub Becton, Dickinson and Company


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