# K172151: Hysteroscopy System

- Pathway: 510(k) (Traditional)
- Applicant: Chongquin Jinshan Science & Technology (Group) Co., Ltd.
- Decided: Apr 9, 2018 after 266 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: 4 generations back to K813282 (1981). 4 ancestors in all.
No later device cites it as a predicate yet.
0 of 5 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K140213: Disposable Endoscopic Cannula, Dongguan Microview Medical Technology Co., Ltd. (2015) Summary page 4.

## Indications for use
The Hysteroscopy System is indicated for rapid transcervical aspiration of the uterine cavity during the first trimester of pregnancy. It has an additional feature of visualization.

Source page: https://510kreport.com/device/K172151
Methodology: https://510kreport.com/methodology