# K233853: LumiGuide Wire; LumiGuide Equipment R2.0; LumiGuide 3D Hub

- Pathway: 510(k) (Special)
- Applicant: Philips Medical Systems Nederland B.V.
- Decided: Mar 14, 2024 after 100 days
- Product code: DQK (Computer, Diagnostic, Programmable)
- Device class: 2
- Regulation: 21 CFR 870.1425
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 7 generations back to K921310 (1992). 15 ancestors in all.
1 later device descends from it; 1 cites it directly.
0 of 17 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K223918: AltaTrack Equipment R1.2, AltaTrack Guidewire, AltaTrack 3D Hub, Philips Medical Systems Nederland B.V. (2023) Summary page 5.

## Most influential descendants
- K252645: LumiGuide Equipment R2.1; LumiGuide Wire; LumiGuide 3D Hub (2025), 0 descendants of its own

## Indications for use
The LumiGuide Wire is an angiographic guidewire with Fiber Optic RealShape (FORS) technology, intended to direct a catheter in endovascular procedures of the peripheral, aortic and aortic side branch vasculature. The LumiGuide Equipment is a visualization device with Fiber Optic RealShape (FORS) technology intended to aid the positioning and navigation of a connected LumiGuide Wire and, optionally, a catheter during endovascular procedures of the peripheral, aortic and aortic side branch vasculature, by creating a 3D image in real-time of the connected LumiGuide Wire and, of an endovascular catheter, when combined with a LumiGuide 3D Hub. The LumiGuide 3D Hub enables the visualization of a connected endovascular catheter, when used in combination with a LumiGuide Wire and the LumiGuide Equipment.

Source page: https://510kreport.com/device/K233853
Methodology: https://510kreport.com/methodology