FDA 510(k) Applications Submitted by BECTON, DICKINSON, AND COMPANY
FDA 510(k) Number |
Submission Date |
Device Name |
Applicant |
K201234 |
05/07/2020 |
BD SoloShot Mini Syringe/ BD Auto Disable Syringe |
Becton, Dickinson, and Company |
K202446 |
08/26/2020 |
BD Preset Syringe & BD A-Line Syringe |
Becton, Dickinson, and Company |
K151589 |
06/12/2015 |
BD MAX CT/GC/TV, BD MAX INSTRUMENT |
BECTON, DICKINSON, AND COMPANY |
K173252 |
10/10/2017 |
BD Phoenix Automated Microbiology System - GN Ceftolozane/tazobactam (0.25/4-32/4 ug/mL) |
Becton, Dickinson, and Company |
K182092 |
08/03/2018 |
BD Intelliport System |
Becton, Dickinson, and Company |
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