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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