# K072387: Karl Storz Video Rhino-Laryngscope System, Model 11101 Series

- Pathway: 510(k) (Traditional)
- Applicant: KARL STORZ Endoscopy-America, Inc.
- Decided: Sep 13, 2007 after 20 days
- Product code: EOB (Nasopharyngoscope (Flexible Or Rigid))
- Device class: 2
- Regulation: 21 CFR 874.4760
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
17 later devices descend from it; 2 cite it directly.
0 of 18 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. The FDA summary names no predicate by number.

## Most influential descendants
- K103467: Cmos Video Rhino-Laryngoscope System Model 11101CM (2012), 10 descendants of its own
- K082569: Entellus Medical Flexible Endoscope and Eyepiece (2008), 5 descendants of its own
- K162916: 3NT endoscopy system (2017), 3 descendants of its own
- K132009: Cmos Video Nasopharyngoscope System (2014), 3 descendants of its own
- K182186: CMOS Video-Rhino-Laryngoscope System (2019), 2 descendants of its own

## Indications for use
The Karl Storz Video Rhino-Laryngoscope System is indicated for use by physicians for endoscopic diagnosis within the nasal lumens and airway anatomy. The endoscope is intended to provide visualization via a video monitor.

Source page: https://510kreport.com/device/K072387
Methodology: https://510kreport.com/methodology