# K936308: Endex Endoscopic Positioning System

- Pathway: 510(k) (Traditional)
- Applicant: Andronic Devices, Ltd.
- Decided: Mar 31, 1994 after 101 days
- Product code: FQO (Table, Operating-Room, Ac-Powered)
- Device class: 1
- Regulation: 21 CFR 878.4960
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
4 later devices descend from it; 1 cites it directly.
0 of 5 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
- K221410: Maestro Platform (2022), 3 descendants of its own
- K240598: Maestro System (REF100) (2024), 2 descendants of its own
- K242323: Maestro System (REF100) (2025), 1 descendant of its own
- K250984: Maestro System (REF100) (2025), 0 descendants of its own

Source page: https://510kreport.com/device/K936308
Methodology: https://510kreport.com/methodology