# K192090: CMOS Video Rhino-Laryngoscope SSU

- Pathway: 510(k) (Traditional)
- Applicant: Karl Storz SE & CO. KG
- Decided: Jan 27, 2020 after 175 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: 3 generations back to K072387 (2007). 3 ancestors in all.
No later device cites it as a predicate yet.
0 of 4 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K182186: CMOS Video-Rhino-Laryngoscope System, KARL STORZ Endoscopy-America, Inc. (2019) Summary page 4.
- K103467: Cmos Video Rhino-Laryngoscope System Model 11101CM, KARL STORZ Endoscopy-America, Inc. (2012) Summary page 4.

## Indications for use
The CMOS Video Rhino‐Laryngoscope SSU is intended to provide visualization of nasal lumens and airway anatomy (including nasopharynx and trachea) during diagnostic procedures. The E‐Box serves as an adaptor for operating the flexible single‐use videoscope on the compatible CCU.

Source page: https://510kreport.com/device/K192090
Methodology: https://510kreport.com/methodology