# K934828: Conmed Universal Plus

- Pathway: 510(k) (Traditional)
- Applicant: Conmedcorp
- Decided: Mar 7, 1994 after 150 days
- Product code: GEI (Electrosurgical, Cutting & Coagulation & Accessories)
- Device class: 2
- Regulation: 21 CFR 878.4400
- 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 lists a 510(k) statement for it but has not posted the file, so its predicates are not known.

## Most influential descendants
- K173112: LAP-iX (2017), 3 descendants of its own
- K200639: LAP-iX (2021), 1 descendant of its own
- K253165: LAP-iX2N (2026), 0 descendants of its own
- K230593: Victan (2023), 0 descendants of its own

Source page: https://510kreport.com/device/K934828
Methodology: https://510kreport.com/methodology