# K800825: Extension Set Quest Code #3000

- Pathway: 510(k) (Traditional)
- Applicant: Quest Medical, Inc.
- Decided: May 14, 1980 after 30 days
- Product code: FPK (Tubing, Fluid Delivery)
- 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
- K151079: Q2 Intravenous Adminstration Sets and Extension Sets (2015), 1 descendant of its own
- K162304: Q2 Multiport IV Administration Sets and Extension Sets, Checkmate Multiport IV Administration Sets, Q2 Extension Sets (2016), 0 descendants of its own

Source page: https://510kreport.com/device/K800825
Methodology: https://510kreport.com/methodology