# K220957: FUJIFILM Endoscope Model EB-710P

- Pathway: 510(k) (Traditional)
- Applicant: Fujifilm Corporaton
- Decided: Nov 10, 2022 after 223 days
- Product code: EOQ (Bronchoscope (Flexible Or Rigid))
- Device class: 2
- Regulation: 21 CFR 874.4680
- 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 K954707 (1995). 4 ancestors in all.
3 later devices descend from it; 3 cite it directly.
0 of 8 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K183607: FUJIFILM Bronchoscope, Fujifilm Corporation (2019) Summary page 4.

## Most influential descendants
- K250863: FUJIFILM Ultrasonic Endoscope EB-710US (2025), 0 descendants of its own
- K244017: FUJIFILM Endoscope Model EB-710P; FUJIFILM Processor EP-8000 (2025), 0 descendants of its own
- K240075: FUJIFILM Endoscope Model EB-710XT (2024), 0 descendants of its own

## Indications for use
FUJIFILM Endoscope Model EB-71 OP is a bronchoscope intended for the observation, diagnosis and endoscopic treatment of the trachea and bronchus at medical facilities under the management of physicians. Never use this product for any other purposes.

Source page: https://510kreport.com/device/K220957
Methodology: https://510kreport.com/methodology