# K253137: FUJIFILM Endoscope Model EB-840S; FUJIFILM Endoscope Model EB-840T

- Pathway: 510(k) (Traditional)
- Applicant: Fujifilm Corporation
- Decided: Jun 16, 2026 after 264 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.
No later device cites it as a predicate yet.
0 of 5 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 5.

## Indications for use
This product is a bronchoscope intended for the observation, diagnosis and endoscopic treatment of the trachea and bronchus at medical facilities under the management of physicians.

Source page: https://510kreport.com/device/K253137
Methodology: https://510kreport.com/methodology