# K170667: QEVO System with KINEVO 900

- Pathway: 510(k) (Traditional)
- Applicant: Carl Zeiss Meditec, AG
- Decided: Aug 18, 2017 after 165 days
- Product code: GWG (Endoscope, Neurological)
- Device class: 2
- Regulation: 21 CFR 882.1480
- 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
- K222735: HJY VisualNext Endoscopic Vision System (2023), 1 descendant of its own
- K243429: HJY VisualNext 3D Endoscopic Vision System (2025), 0 descendants of its own
- K232159: QEVO System (2023), 0 descendants of its own

Source page: https://510kreport.com/device/K170667
Methodology: https://510kreport.com/methodology