# K170975: Televere Digital Imaging System

- Pathway: 510(k) (Traditional)
- Applicant: Televere Systems
- Decided: May 1, 2017 after 28 days
- Product code: MQB (Solid State X-Ray Imager (Flat Panel/Digital Imager))
- 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: 9 generations back to K981556 (1998). 20 ancestors in all.
2 later devices descend from it; 2 cite it directly.
0 of 23 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K123644: Vizion + DR, Viztek, LLC (2013) Summary page 4.

## Most influential descendants
- K180765: Televere Podiatry X-Ray System HF (2018), 0 descendants of its own
- K172124: Televere Podiatry Digital Imaging System (2017), 0 descendants of its own

## Indications for use
The Televere Digital Imaging System is intended for digital image capture use in general radiographic examinations, wherever conventional screen-film systems may be used. Allows imaging of the skull, chest, shoulders, spine, abdomen, pelvis, and extremities. Not for mammography.

Source page: https://510kreport.com/device/K170975
Methodology: https://510kreport.com/methodology