# K790692: Televix

- Pathway: 510(k) (Traditional)
- Applicant: General Electrical Espanola, S.A.
- Decided: Apr 23, 1979 after 13 days
- Product code: KXJ (Table, Radiologic)
- Device class: 2
- Regulation: 21 CFR 892.1980
- Recalls of this device: 1 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
8 later devices descend 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)
- None. FDA has not posted a summary or statement for it, so its predicates are not known.

## Most influential descendants
- K071546: EOS (2007), 7 descendants of its own
- K120721: EOS (2012), 6 descendants of its own
- K123740: EOS (2013), 5 descendants of its own
- K142773: EOS System (2015), 4 descendants of its own
- K152788: EOS System (2015), 3 descendants of its own

## Recalls of this device
- Mar 29, 2019 · Class II · Z-1753-2019: There has been a reported incident of a Distar CRT monitor that has fallen off the monitor wall mount related to product aging.

Source page: https://510kreport.com/device/K790692
Methodology: https://510kreport.com/methodology