# K151567: ENDOPLUS hand-held laparoscopic instruments

- Pathway: 510(k) (Traditional)
- Applicant: Endoplus
- Decided: Dec 23, 2015 after 196 days
- Product code: HFI (Coagulator, Culdoscopic (And Accessories))
- Device class: 2
- Regulation: 21 CFR 884.4160
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 3 generations back to K935270 (1994). 3 ancestors in all.
1 later device descends 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)
- K062072: Pajunks Disposable Inserts for Handle Instruments and HF Electrodes, PAJUNK GmbH Medizintechnologie (2006) Summary page 4.

## Most influential descendants
- K193018: Surgical Direct Hand-held Laparoscopic Instruments (2019), 0 descendants of its own

## Indications for use
Endoplus Hand held Laparoscopic instruments are intended for grasping, cutting, dissecting, retracting, clamping, biopsy, and/or cauterization of tissue. The devices are used in conjunction with a laparoscope during laparoscopic procedures. Instruments should be used only by personnel completely familiar with their operation. Using an instrument improperly for a task which it was not intended may result in a damaged or broken instrument.

Source page: https://510kreport.com/device/K151567
Methodology: https://510kreport.com/methodology