# K103467: Cmos Video Rhino-Laryngoscope System Model 11101CM

- Pathway: 510(k) (Special)
- Applicant: KARL STORZ Endoscopy-America, Inc.
- Decided: Jun 28, 2012 after 582 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
Longest line of descent: 1 generation back to K072387 (2007). 1 ancestor in all.
10 later devices descend from it; 6 cite it directly.
0 of 12 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K072387: Karl Storz Video Rhino-Laryngscope System, Model 11101 Series, KARL STORZ Endoscopy-America, Inc. (2007) Summary page 1.

## Most influential descendants
- K132009: Cmos Video Nasopharyngoscope System (2014), 3 descendants of its own
- K182186: CMOS Video-Rhino-Laryngoscope System (2019), 2 descendants of its own
- K200609: ENTity WiFi Video Nasopharyngoscope System (2021), 1 descendant of its own
- K143673: CMOS Video Nasopharyngoscope System (2015), 1 descendant of its own
- K254133: ENTity USB Videoscope System (2026), 0 descendants of its own

## Indications for use
The KARL STORZ CMOS Flexible Video Rhino- Laryngoscope System may only be used by persons with an appropriate medical qualification and who are acquainted with the rhino/laryngoscopic technique. The endoscope is used for endoscopic diagnosis within the nasal lumens and airway anatomy, and is intended to provide visualization via a video monitor.

Source page: https://510kreport.com/device/K103467
Methodology: https://510kreport.com/methodology