# K183607: FUJIFILM Bronchoscope

- Pathway: 510(k) (Traditional)
- Applicant: Fujifilm Corporation
- Decided: Aug 23, 2019 after 240 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: 3 generations back to K954707 (1995). 3 ancestors in all.
5 later devices descend from it; 2 cite it directly.
0 of 9 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K122535: Fujinon/Fujifilm EB-530 Series Bronchoscopes (EB-530S, EB-530T and EB-530H, Fujifilm Medical System U.S.A., Inc. (2012) Summary page 4.

## Most influential descendants
- K220957: FUJIFILM Endoscope Model EB-710P (2022), 3 descendants of its own
- K253137: FUJIFILM Endoscope Model EB-840S; FUJIFILM Endoscope Model EB-840T (2026), 0 descendants of its own
- 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 Bronchoscopes EB-580S and EB-580T are intended for the observation, diagnosis, and endoscopic treatment of the trachea and bronchial tree.

Source page: https://510kreport.com/device/K183607
Methodology: https://510kreport.com/methodology