Becton, Dickinson and Company - FDA 510(k) Cleared Devices
Recent clearances: BD Preset™ and BD A-Line™ Arterial Blood Collection Syringes, BD® MiniDraw™ Capillary Blood Collection System with BD® MiniDraw™ SST™ Capillary Blood Collection Tube, BD Vacutainer® Safety-Lok™ Blood Collection Set
134
Total
134
Cleared
0
Denied
FDA 510(k) Regulatory Record - Becton, Dickinson and Company General Hospital ✕
55 devices
Cleared
Apr 10, 2026
BD Vacutainer® Safety-Lok™ Blood Collection Set
General Hospital
245d
Cleared
Dec 02, 2025
0.9 % Sodium Chloride Injection, USP, BD PosiFlush™ SP Syringe
General Hospital
253d
Cleared
Sep 12, 2025
BD PhaSeal™ Optima Connecting Set (C83-O)
General Hospital
245d
Cleared
Jul 29, 2025
BD Plastipak™ Syringe
General Hospital
90d
Cleared
Jul 03, 2025
BD Vacutainer® Eclipse™ Blood Collection Needle
General Hospital
275d
Cleared
Mar 21, 2025
BD Vacutainer® Multiple Sample Luer Adapter
General Hospital
115d
Cleared
Nov 01, 2024
BD Vacutainer® One Use Holder
General Hospital
88d
Cleared
Jul 21, 2023
0.9% Sodium Chloride Injection, USP BD PosiFlush™ SF Saline Flush Syringe
General Hospital
88d
Cleared
Mar 24, 2023
BD Vacutainer® Push Button Blood Collection Set, BD Vacutainer® Push Button...
General Hospital
422d
Cleared
Mar 10, 2023
BD Vacutainer® Luer-Lok™ Access Device, BD Vacutainer® Blood Transfer Device
General Hospital
206d
Cleared
Dec 28, 2022
BD AutoShield Duo™ Pen Needle
General Hospital
64d
Cleared
Jul 16, 2022
0.9% Sodium Chloride Injection, USP, BD PosiFlush SafeScrub
General Hospital
211d
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