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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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