BD PosiFlush Heparin Lock Flush Syringe
K-Number: K163591 · 2017-02-27
ApplicantBecton, Dickinson and Company
Decision Date2017-02-27
Product CodeNZW
Advisory CommitteeHO
DecisionSubstantially Equivalent
Device Summary
BD PosiFlush Heparin Lock Flush Syringe is a medical device manufactured by Becton, Dickinson and Company. It received FDA 510(k) clearance on 2017-02-27 under approval number K163591. The device is classified under product code NZW. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the BD PosiFlush Heparin Lock Flush Syringe?
BD PosiFlush Heparin Lock Flush Syringe is a medical device that received FDA 510(k) clearance on 2017-02-27. It is manufactured by Becton, Dickinson and Company. The 510(k) number is K163591.
When was BD PosiFlush Heparin Lock Flush Syringe approved by the FDA?
BD PosiFlush Heparin Lock Flush Syringe received FDA 510(k) clearance on 2017-02-27, under approval number K163591.
What company makes BD PosiFlush Heparin Lock Flush Syringe?
BD PosiFlush Heparin Lock Flush Syringe is manufactured by Becton, Dickinson and Company.
What is the FDA product code for BD PosiFlush Heparin Lock Flush Syringe?
The FDA product code for BD PosiFlush Heparin Lock Flush Syringe is NZW.
Other Devices by Becton, Dickinson and Company
K162081BD 1ml Luer-lok Hypodermic Syringe, BD 1 mL Luer-Lok Hypodermic Syringe with BD Hypodermic Needle or BD Eclipse Hypodermic Needle, BD 1ml Luer-lok Insulin Syringe
K162516BD Pen Needle
K160657BD Vacutainer Barricor Lithium Heparin Plasma Blood Collection Tube
K151589BD MAX CT/GC/TV, BD MAX INSTRUMENT
K151870BD U-500 INSULIN SYRINGE
K161553BD SafeAssist
Official Source
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.