# K091377: BD Flu+ Syringe

- Pathway: 510(k) (Traditional)
- Applicant: Becton, Dickinson & CO
- Decided: Jul 2, 2009 after 52 days
- Product code: FMF (Syringe, Piston)
- Device class: 2
- Regulation: 21 CFR 880.5860
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 2 generations back to K883955 (1988). 2 ancestors in all.
1 later device descends from it; 1 cites it directly.
0 of 4 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K042934: 1BD Soloshot IX Syringe, Becton, Dickinson & CO (2004) Summary page 1.

## Most influential descendants
- K203359: BD Flu+ Syringe (2021), 0 descendants of its own

## Indications for use
The BD Flu+ Syringes are intended for the aspiration and injection of the influenza vaccine.

Source page: https://510kreport.com/device/K091377
Methodology: https://510kreport.com/methodology