Bd

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
15
Inspections
2
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K253445BD Surgiphor™ 1000 mL Antimicrobial Irrigation System (910120)February 20, 2026
K240257Denali™ Vena Cava Filter System – Femoral and Jugular/Subclavian Delivery KitFebruary 29, 2024
K232434BD Veritor™ System for Rapid Detection of Flu A+B CLIA Waived KitDecember 5, 2023
K223016BD VeritorTM System for Rapid Detection of Flu A+B CLIA-Waived KitJanuary 27, 2023
K221504BD Surgiphor™ Antimicrobial Irrigation SystemOctober 14, 2022
K180438BD Veritor System for Rapid Detection of Flu A + B CLIA waived kitMarch 20, 2018
K024240BD VACUTAINER PLUS PLASTIC URINE C&S PRESERVAYIVE TUBES AND KITSMarch 26, 2003
K023752BD INTEGRA SYRINGEFebruary 7, 2003
K021475BD SINGLE LUMEN NEEDLE, SYRINGE AND BLOOD COLLECTION SETJuly 19, 2002
K020523BD BIFURCATED NEEDLE, MODELS 301754, 301755, 301756, 301757March 20, 2002
K011967BD PRE-FILLED HEPARIN LOCK FLUSH IN 0.9% SODIUM CHLORIDE INJECTION, USP SYRINGEJanuary 23, 2002
K012584MODIFICATION TO: BD DURASAFE PLUS EPIDURAL LOCK CSE NEEDLE SET/KITSeptember 6, 2001
K0119820.9% SODIUM CHLORIDE INJECTION, USP BD PRE-FILLED FLUSH SYRINGEJuly 17, 2001
K011858INTERLINK THREADED LOCK CANNULAJune 19, 2001
K011103BD SPRING BASED SYRINGEJune 13, 2001