# K993893: Medx Intecam Interface

- Pathway: 510(k) (Traditional)
- Applicant: Medx, Inc.
- Decided: Feb 10, 2000 after 86 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 K904174 (1991). 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)
- K904174: Starcam 4000, General Electric Co. (1991) Summary page 1.

## Indications for use
The intended uses of the MEDX InteCam™ Interface accessory together with the NuQuest™ Nuclear Medicine Computer 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/K993893
Methodology: https://510kreport.com/methodology