# K113241: BD Emerald Single Use, Hypodermic Syringe

- Pathway: 510(k) (Special)
- Applicant: Becton Dickinson
- Decided: Nov 28, 2011 after 26 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 K980987 (1998). 2 ancestors in all.
2 later devices descend from it; 2 cite it directly.
0 of 5 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K980987: Becton Dickinson Syringe, Bd Becton Dickinson Vacutainer Systems Preanalytic (1998) Summary page 1.
- K110771: BD Single Use, Hypodermic Syringe, Becton, Dickinson and Company (2011) Summary page 1.

## Most influential descendants
- K210914: Sterile Syringe for Single Use (2021), 0 descendants of its own
- K121283: BD Emerald Saf-T Single Use, Hypodermic (2012), 0 descendants of its own

## Indications for use
The BD Emerald Single Use, Hypodermic Syringe is intended for use by health care professionals for general purpose aspiration and injection of fluids.

Source page: https://510kreport.com/device/K113241
Methodology: https://510kreport.com/methodology