# K212950: FUJIFILM Video Laparoscope EL-R740M30

- Pathway: 510(k) (Traditional)
- Applicant: Fujifilm Corporaton
- Decided: Dec 2, 2021 after 77 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: 13 generations back to K931154 (1993). 39 ancestors in all.
No later device cites it as a predicate yet.
3 of 40 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K202130: FUJIFILM Video Laparoscope, Fujifilm Corporation (2020) Summary page 4.

## Indications for use
FUJIFILM Video Laparoscope EL-R740M30 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/K212950
Methodology: https://510kreport.com/methodology