# K240075: FUJIFILM Endoscope Model EB-710XT

- Pathway: 510(k) (Special)
- Applicant: FUJIFILM Healthcare Americas Corporation
- Decided: Feb 7, 2024 after 28 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: 5 generations back to K954707 (1995). 5 ancestors in all.
No later device cites it as a predicate yet.
0 of 6 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K220957: FUJIFILM Endoscope Model EB-710P, Fujifilm Corporaton (2022) Summary page 5.

## Indications for use
Endoscope Model EB-710XT 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/K240075
Methodology: https://510kreport.com/methodology