# K000685: Charter Medical Neonatal Syringe Set

- Pathway: 510(k) (Traditional)
- Applicant: Charter Medical, Ltd.
- Decided: Aug 15, 2000 after 168 days
- Product code: BRZ (Set, Blood Transfusion)
- Device class: 2
- Regulation: 21 CFR 880.5440
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
2 later devices descend from it; 2 cite it directly.
0 of 3 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
- K132905: 200 Micron Blood Component Filter and Syringe Adapter (2013), 0 descendants of its own
- K050805: 30 ML or 60 ML Pedi-Syringe Filter (2005), 0 descendants of its own

Source page: https://510kreport.com/device/K000685
Methodology: https://510kreport.com/methodology