# K884212: Winged Non-Coring Needle Set

- Pathway: 510(k) (Traditional)
- Applicant: Marquette Medical, Inc.
- Decided: Oct 17, 1988 after 11 days
- Product code: FMI (Needle, Hypodermic, Single Lumen)
- Device class: 2
- Regulation: 21 CFR 880.5570
- Recalls of this device: none
- 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
- K981683: Huber Needle Infusion Set Model #20G01 & Y-Site Model #20G01Y (1998), 0 descendants of its own

Source page: https://510kreport.com/device/K884212
Methodology: https://510kreport.com/methodology