# K954707: Bronchoscope

- Pathway: 510(k) (Traditional)
- Applicant: Fujinon, Inc.
- Decided: Nov 22, 1995 after 41 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
No predicates in its family tree.
9 later devices descend from it; 1 cites 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)
- None. FDA lists a 510(k) statement for it but has not posted the file, so its predicates are not known.

## Most influential descendants
- K050907: Fujinon G5 Bronchoscopes, Models EB-470S, EB-250S, and EB-270P (2005), 8 descendants of its own
- K122535: Fujinon/Fujifilm EB-530 Series Bronchoscopes (EB-530S, EB-530T and EB-530H (2012), 7 descendants of its own
- 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

Source page: https://510kreport.com/device/K954707
Methodology: https://510kreport.com/methodology