# K171229: DELL UP3017 with QUBYX PerfectLum bundle

- Pathway: 510(k) (Traditional)
- Applicant: Qubyx Software Technologies, Inc.
- Decided: May 26, 2017 after 29 days
- Product code: PGY (Display, Diagnostic Radiology)
- Device class: 2
- Regulation: 21 CFR 892.2050
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 6 generations back to K040982 (2004). 7 ancestors in all.
1 later device descends from it; 1 cites it directly.
0 of 9 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K131601: Dell U3014 with Qubyx Perfectlum Bundle, Qubyx Limited (2014) Summary page 4.

## Most influential descendants
- K200889: iMac 27 & PL 4.0 (2020), 0 descendants of its own

## Indications for use
The DELL UP3017 with QUBYX PerfectLum is intended to be used for displaying and viewing medical images, for review and analysis by trained medical practitioners. The DELL UP3017 can be used only in conjunction with QUBYX PerfectLum. The device can not be used in primary image diagnosis in mammography. The device can not be used for a life-support system. The device does not contact with the patient. The device is intended for prescription use.

Source page: https://510kreport.com/device/K171229
Methodology: https://510kreport.com/methodology