# K011103: BD Spring Based Syringe

- Pathway: 510(k) (Traditional)
- Applicant: Bd
- Decided: Jun 13, 2001 after 63 days
- Product code: MEG (Syringe, Antistick)
- 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.
99 later devices descend from it; 4 cite it directly.
0 of 100 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
- K053519: Safety Syringe (2006), 79 descendants of its own
- K072739: Jierui Syringes and Needles (2008), 78 descendants of its own
- K110421: Disposable Insulin Syringe (2011), 36 descendants of its own
- K112057: KDL Syringes and Needle (2011), 31 descendants of its own
- K023752: BD Integra Syringe (2003), 16 descendants of its own

Source page: https://510kreport.com/device/K011103
Methodology: https://510kreport.com/methodology