# K171825: Disposable Endoscopic Surgical Instrument, Reusable Endoscopic Surgical Instrument

- Pathway: 510(k) (Traditional)
- Applicant: Hunan Handlike Minimally Invasive Surgery Co., Ltd.
- Decided: Feb 13, 2018 after 239 days
- Product code: GEI (Electrosurgical, Cutting & Coagulation & Accessories)
- Device class: 2
- Regulation: 21 CFR 878.4400
- 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 K910831 (1991). 10 ancestors in all.
1 later device descends from it; 1 cites it directly.
0 of 12 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K132771: Kingston Endoscopic Surgical Instruments, Qingdao Kingston Medical Devices, Ltd. (2014) Summary page 5.
- K102921: Endoscopic Monopolar Instruments and Accessories, Bema-GmbH & Co. KG (2011) Summary page 5.

## Most influential descendants
- K211019: Disposable Monopolar Laparoscopic Tips and Reusable Handles (2021), 0 descendants of its own

## Indications for use
Endoscopic Instruments are designed to cut, dissect, manipulate and/or cauterize various tissues during endoscopic/laparoscopic, general surgical procedures.

Source page: https://510kreport.com/device/K171825
Methodology: https://510kreport.com/methodology