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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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