# K231721: Disposable Hot Biopsy Forceps

- Pathway: 510(k) (Traditional)
- Applicant: Beijing Zksk Technology Co., Ltd.
- Decided: Dec 14, 2023 after 184 days
- Product code: KGE (Forceps, Biopsy, Electric)
- Device class: 2
- Regulation: 21 CFR 876.4300
- 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 K955052 (1996). 3 ancestors in all.
No later device cites it as a predicate yet.
0 of 4 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K062517: Electrosurgical Hemostatic Forceps Series, Olympus Medical Systems Corporation (2006) Summary page 6.

## Indications for use
This instrument has been designed to be used with endoscopes to collect tissue,cauterize,coagulate and perform hemostasis using high-frequency current within the digestive tract.

Source page: https://510kreport.com/device/K231721
Methodology: https://510kreport.com/methodology