BD Flu+ Syringe
K-Number: K203359 · 2021-07-28
Device Summary
Frequently Asked Questions
What is the BD Flu+ Syringe?
BD Flu+ Syringe is a medical device that received FDA 510(k) clearance on 2021-07-28. It is manufactured by Becton, Dickinson and Company. The 510(k) number is K203359.
When was BD Flu+ Syringe approved by the FDA?
BD Flu+ Syringe received FDA 510(k) clearance on 2021-07-28, under approval number K203359.
What company makes BD Flu+ Syringe?
BD Flu+ Syringe is manufactured by Becton, Dickinson and Company.
What is the FDA product code for BD Flu+ Syringe?
The FDA product code for BD Flu+ Syringe is FMF.
Other Devices by Becton, Dickinson and Company
Related Devices (Code: FMF)
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.