# K041840: Medx Nuquest - Intecam Spect 37-75 System

- Pathway: 510(k) (Traditional)
- Applicant: Medx, Inc.
- Decided: Aug 20, 2004 after 43 days
- Product code: KPS (System, Tomography, Computed, Emission)
- Device class: 2
- Regulation: 21 CFR 892.1200
- 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 K953255 (1995). 1 ancestor in all.
No later device cites it as a predicate yet.
0 of 2 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K953255: Nuquest Nuclear Medicine Computer, Sitco, Inc. (1995). Our reading of the summary gave “K953255.The” beside “510(k)”; FDA’s K953255 is the only number that fits it and carries the summary’s name for the device. Summary page 2.

## Indications for use
The intended uses of the MEDX NuQuest™ InteCam™ SPECT 37-75 System are the acquisition, processing, display and analysis of planar and SPECT nuclear images of all organ systems using approved pharmaceuticals.

Source page: https://510kreport.com/device/K041840
Methodology: https://510kreport.com/methodology