# K142011: Solution Set/Extension Set

- Pathway: 510(k) (Special)
- Applicant: Baxter Healthcare Corporation
- Decided: Aug 18, 2014 after 25 days
- Product code: FPA (Set, Administration, Intravascular)
- 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
Longest line of descent: 1 generation back to K811078 (1981). 2 ancestors in all.
1 later device descends from it; 1 cites it directly.
0 of 4 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K811078: Radiation Sterilized Admin. Set, Travenol Laboratories, S.A. (1981) Summary page 5.
- K961225: Continuflo Solution Set/Secondary Medication Set, Baxter Healthcare Corp (1996) Summary page 5.

## Most influential descendants
- K150860: Nitroglycerin Sets with DUO-VENT Spike (2015), 0 descendants of its own

## Indications for use
For the administration of fluids from a container into the patient’s vascular system through a vascular access device.

Source page: https://510kreport.com/device/K142011
Methodology: https://510kreport.com/methodology