# K141366: Video Bronchoscope System

- Pathway: 510(k) (Traditional)
- Applicant: Scholly Fiberoptic GmbH
- Decided: Dec 17, 2014 after 208 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: 1 generation back to K071530 (2007). 1 ancestor in all.
13 later devices descend from it; 1 cites it directly.
0 of 15 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K071530: Karl Storz Video Flexible Video Ent Endoscope System, KARL STORZ Endoscopy-America, Inc. (2007) Summary page 4.

## Most influential descendants
- K182188: Ion Endoluminal System ; Flexision Biopsy Needle (2019), 12 descendants of its own
- K202370: Ion Endoluminal System (2020), 5 descendants of its own
- K220299: Ion Endoluminal System (IF1000) (2022), 4 descendants of its own
- K232984: Ion Endoluminal System (IF1000) (2023), 3 descendants of its own
- K192367: Ion Endoluminal System (2019), 3 descendants of its own

## Indications for use
The Schoelly Video Bronchoscope System is intended for use by physicians for diagnostic and therapeutic procedures in nasopharyngeal endoscopy, bronchoscopy, tracheoscopy, and laryngoscopy. The Schoelly Video Bronchoscope is intended to provide visualization via a video monitor.

Source page: https://510kreport.com/device/K141366
Methodology: https://510kreport.com/methodology