# K093556: Vcare DX

- Pathway: 510(k) (Traditional)
- Applicant: Conmed Corporation
- Decided: Mar 12, 2010 after 115 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: 1 generation back to K955446 (1996). 1 ancestor in all.
1 later device descends from it; 1 cites it directly.
0 of 3 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K955446: Conmed Vcare Retractor/Elevator, Conmedcorp (1996) Summary page 1.

## Most influential descendants
- K172846: Uterine Manipulator (2018), 0 descendants of its own

## Indications for use
VCARE Dx uterine manipuilator/injector cannula is indicated for manipulation of the uterus, and injection of fluids during laparoscopic gynecologic procedures such as laparoscopic supracervical hysterectomy, minilap tubal ligation, laparoscopic tubal occlusion or diagnostic laparoscopy.

Source page: https://510kreport.com/device/K093556
Methodology: https://510kreport.com/methodology