# K190611: Vivix-S 1751S

- Pathway: 510(k) (Traditional)
- Applicant: Vieworks Co., Ltd.
- Decided: Apr 8, 2019 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
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. The FDA summary names no predicate by number.

## Most influential descendants
- K220536: Digital flat panel detector (2022), 1 descendant of its own
- K241125: Vivix-S 1751S (2024), 0 descendants of its own
- K230059: Digital Flat Panel Detector (2023), 0 descendants of its own

Source page: https://510kreport.com/device/K190611
Methodology: https://510kreport.com/methodology
