# K944931: Becton Dickinson Blunt Steel Cannula

- Pathway: 510(k) (Traditional)
- Applicant: Bd Becton Dickinson Vacutainer Systems Preanalytic
- Decided: Aug 29, 1995 after 327 days
- Product code: FMI (Needle, Hypodermic, Single Lumen)
- Device class: 2
- Regulation: 21 CFR 880.5570
- Recalls of this device: 1 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
1 later device descends from it; 1 cites it directly.
0 of 2 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. FDA has not posted a summary or statement for it, so its predicates are not known.

## Most influential descendants
- K131842: Sterican Cannula (2013), 0 descendants of its own

## Recalls of this device
- Dec 19, 2014 · Class II · Z-1055-2015: The stopper of the 10mL BD Luer-Lok syringe is not properly seated in the syringe.

Source page: https://510kreport.com/device/K944931
Methodology: https://510kreport.com/methodology