# K093508: Rigid Cannulae Curved (RC6-RC12), Rigid Cannulae Straight (RS6-RS12)

- Pathway: 510(k) (Traditional)
- Applicant: Womancare Global
- Decided: Mar 4, 2010 after 112 days
- Product code: HGH (Cannula, Suction, Uterine)
- Device class: 2
- Regulation: 21 CFR 884.5070
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 2 generations back to K813282 (1981). 2 ancestors in all.
2 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)
- K030935: Berkeley V-10 Vacuum Curettage System, Acmi Corporation (2003) Summary page 1.
- K813282: Synevac Vacuum Curettage Systems, Synemed, Inc. (1981) Summary page 1.

## Most influential descendants
- K140213: Disposable Endoscopic Cannula (2015), 1 descendant of its own
- K172151: Hysteroscopy System (2018), 0 descendants of its own

## Indications for use
For rapid transcervical aspiration of the uterine cavity during the first trimester of pregnancy.

Source page: https://510kreport.com/device/K093508
Methodology: https://510kreport.com/methodology