# K172592: CADD Yellow High Volume Administration Set with NRFit connector

- Pathway: 510(k) (Traditional)
- Applicant: Smiths Medical Asd, Inc.
- Decided: May 17, 2018 after 261 days
- Product code: PWH (Administrations Sets With Neuraxial Connectors)
- 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 K031361 (2003). 1 ancestor in all.
1 later device descends from it; 1 cites it directly.
1 of 3 devices in its family (counting itself) has a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K031361: Cadd High-Volume Administration Sets with Flowstop, Deltec, Inc. (2003) Summary page 4.

## Most influential descendants
- K221319: BD Alaris™ Pump Epidural Infusion Set (2023), 0 descendants of its own

## Indications for use
CADD® Yellow High Volume Administration Sets with NRFit™ connectors are designed for use only with NRFit™ components for delivery of regional anesthetics or narcotics, excluding subarachnoid/spinal block, and are designed for use with CADD® pumps (see CADD® pump Operator’s Manual for compatibility). The intended population is pediatrics and adults.

Source page: https://510kreport.com/device/K172592
Methodology: https://510kreport.com/methodology