# K182244: Voyant Electrosurgical Generator

- Pathway: 510(k) (Special)
- Applicant: Applied Medical Resources Corp.
- Decided: Oct 11, 2018 after 52 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
Longest line of descent: 5 generations back to K932293 (1994). 13 ancestors in all.
1 later device descends from it; 1 cites it directly.
0 of 15 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K141288: Voyant Electrosurgical Generator, Voyant 5MM Laparoscopic Sealer-Divider Device, Applied Medical Resources (2014) Summary page 4.

## Most influential descendants
- K252412: Voyant® Electrosurgical Generator (EA030/Electrosurgical Generator) (2025), 0 descendants of its own

## Indications for use
The Voyant electrosurgical generator is indicated for use with Voyant devices in open and laparoscopic surgical procedures where the electrosurgical ligation of vessels or tissue bundles is desired. Note: For indications specific to each Voyant device used with the Voyant generator, refer to each device’s Instructions for Use (IFU).

Source page: https://510kreport.com/device/K182244
Methodology: https://510kreport.com/methodology