# K052473: CX 250 C Plus with Gammaxp Software, Model 0121 0000

- Pathway: 510(k) (Traditional)
- Applicant: Inter Medical Medizintechnik GmbH
- Decided: Oct 28, 2005 after 49 days
- Product code: IYX (Camera, Scintillation (Gamma))
- Device class: 1
- Regulation: 21 CFR 892.1100
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
3 later devices descend from it; 2 cite it directly.
0 of 4 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. FDA has not posted a summary or statement for it, so its predicates are not known.

## Most influential descendants
- K073456: T-Quest System (2007), 1 descendant of its own
- K132347: Multicam 3000 Eco (2013), 0 descendants of its own
- K101391: Scandia-45 Gamma Camera System (2010), 0 descendants of its own

Source page: https://510kreport.com/device/K052473
Methodology: https://510kreport.com/methodology