# K202130: FUJIFILM Video Laparoscope

- Pathway: 510(k) (Special)
- Applicant: Fujifilm Corporation
- Decided: Aug 20, 2020 after 20 days
- Product code: GCJ (Laparoscope, General & Plastic Surgery)
- Device class: 2
- Regulation: 21 CFR 876.1500
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 12 generations back to K931154 (1993). 38 ancestors in all.
1 later device descends from it; 1 cites it directly.
3 of 40 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K192918: Video Laparoscope, Video Processor, Light Source, Fujifilm Corporation (2020) Summary page 4.

## Most influential descendants
- K212950: FUJIFILM Video Laparoscope EL-R740M30 (2021), 0 descendants of its own

## Indications for use
FUJIFILM Video Laparoscope EL-R740M is intended to be used with a video processor, light source, monitor, hand instruments, electrosurgical unit and other ancillary equipment for minimally invasive observation, diagnosis and treatment in general abdominal, gynecologic and thoracic areas.

Source page: https://510kreport.com/device/K202130
Methodology: https://510kreport.com/methodology