# K122820: Viky UP

- Pathway: 510(k) (Traditional)
- Applicant: Endocontrol
- Decided: Jun 18, 2013 after 277 days
- Product code: LKF (Cannula, Manipulator/Injector, Uterine)
- Device class: 2
- Regulation: 21 CFR 884.4530
- 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 K931783 (1993). 9 ancestors in all.
No later device cites it as a predicate yet.
0 of 10 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K082233: VIKY, Endocontrol (2008) Summary page 1.
- K071405: Probe Holder System, Intuitive Surgical, Inc. (2007) Summary page 1.

## Indications for use
The VIKY UP device is indicated for computer-controlled laparoscopic hysterectomies (such as da Vinci-assisted laparoscopic hysterectomies) for the purpose of holding and controlling the movement of a uterine manipulator.

Source page: https://510kreport.com/device/K122820
Methodology: https://510kreport.com/methodology