# K941562: 1ML Luer-Lok Syringe

- Pathway: 510(k) (Traditional)
- Applicant: Bd Becton Dickinson Vacutainer Systems Preanalytic
- Decided: May 26, 1994 after 55 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
No predicates in its family tree.
5 later devices descend from it; 4 cite it directly.
0 of 6 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
- K162081: BD 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 (2016), 1 descendant of its own
- K243322: Altaviz Intravitreal Syringe (2025), 0 descendants of its own
- K222852: Nipro SafeTouch Needle; Nipro Syringe with SafeTouch Needle (2023), 0 descendants of its own
- K062865: Small Volume Syringe (2007), 0 descendants of its own
- K022495: Gettig Disposable Syringes (2002), 0 descendants of its own

Source page: https://510kreport.com/device/K941562
Methodology: https://510kreport.com/methodology