# K110849: Prestodr 4143

- Pathway: 510(k) (Special)
- Applicant: Cmt Medical Technologies, Ltd.
- Decided: Apr 26, 2011 after 29 days
- Product code: KPR (System, X-Ray, Stationary)
- Device class: 2
- Regulation: 21 CFR 892.1680
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 4 generations back to K931071 (1994). 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)
- K100400: Prestodr Portable, Cmt Medical Technologies, Ltd. (2010) Summary page 1.

## Most influential descendants
- K162224: ArtPix Mobile EZ2GO (2016), 0 descendants of its own

## Indications for use
The PrestoDR 4143™, is intended for use in general radiographic examinations, wherever conventional screen-film systems may be used, excluding fluoroscopy, angiography and mammography. PrestoDR 4143™ allows imaging of the skull, chest, shoulders, spine, abdomen, and extremities.

Source page: https://510kreport.com/device/K110849
Methodology: https://510kreport.com/methodology