# K082233: VIKY

- Pathway: 510(k) (Traditional)
- Applicant: Endocontrol
- Decided: Dec 18, 2008 after 133 days
- Product code: GCJ (Laparoscope, General & Plastic Surgery)
- Device class: 2
- Regulation: 21 CFR 876.1500
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 4 generations back to K931783 (1993). 5 ancestors in all.
1 later device descends from it; 1 cites it directly.
0 of 7 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K972699: Aesop 3000 System and Accessories, Computer Motion, Inc. (1997) Summary page 1.
- K050027: Laparocision Scope Controller System, Gmp/Companies, Inc. (2005) Summary page 1.

## Most influential descendants
- K122820: Viky UP (2013), 0 descendants of its own

## Indications for use
The ViKY System is indicated for thoracic and laparoscopic minimally invasive procedures for the purpose of holding and controlling the movement of standard rigid endoscopes within surgical cavities during endoscopic surgery.

Source page: https://510kreport.com/device/K082233
Methodology: https://510kreport.com/methodology