FDA 510(k) Applications Submitted by BD

FDA 510(k) Number Submission Date Device Name Applicant
K180438 02/20/2018 BD Veritor System for Rapid Detection of Flu A + B CLIA waived kit BD
K223016 09/29/2022 BD VeritorTM System for Rapid Detection of Flu A+B CLIA-Waived Kit BD
K011103 04/11/2001 BD SPRING BASED SYRINGE BD
K011858 06/14/2001 INTERLINK THREADED LOCK CANNULA BD
K011967 06/25/2001 BD PRE-FILLED HEPARIN LOCK FLUSH IN 0.9% SODIUM CHLORIDE INJECTION, USP SYRINGE BD
K011982 06/26/2001 0.9% SODIUM CHLORIDE INJECTION, USP BD PRE-FILLED FLUSH SYRINGE BD
K024240 12/23/2002 BD VACUTAINER PLUS PLASTIC URINE C&S PRESERVAYIVE TUBES AND KITS BD
K021475 05/08/2002 BD SINGLE LUMEN NEEDLE, SYRINGE AND BLOOD COLLECTION SET BD
K012584 08/10/2001 MODIFICATION TO: BD DURASAFE PLUS EPIDURAL LOCK CSE NEEDLE SET/KIT BD
K023752 11/08/2002 BD INTEGRA SYRINGE BD
K020523 02/19/2002 BD BIFURCATED NEEDLE, MODELS 301754, 301755, 301756, 301757 BD
K221504 05/23/2022 BD SurgiphorÖ Antimicrobial Irrigation System BD


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