# K122535: Fujinon/Fujifilm EB-530 Series Bronchoscopes (EB-530S, EB-530T and EB-530H

- Pathway: 510(k) (Traditional)
- Applicant: Fujifilm Medical System U.S.A., Inc.
- Decided: Dec 13, 2012 after 115 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: 2 generations back to K954707 (1995). 2 ancestors in all.
7 later devices descend from it; 2 cite it directly.
0 of 10 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K050907: Fujinon G5 Bronchoscopes, Models EB-470S, EB-250S, and EB-270P, Fujinon, Inc. (2005) Summary page 3.

## Most influential descendants
- K183607: FUJIFILM Bronchoscope (2019), 5 descendants of its own
- 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

## Indications for use
This device is intended for the observation, diagnosis, and endoscopic treatment of the trachea and bronchial tree.

Source page: https://510kreport.com/device/K122535
Methodology: https://510kreport.com/methodology