# K200740: HD Video Rhino Laryngoscope

- Pathway: 510(k) (Traditional)
- Applicant: KARL STORZ Endoscopy-America, Inc.
- Decided: Aug 11, 2020 after 141 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 KARL STORZ CMOS HD Video Rhino-Laryngoscope System is indicated to provide visualization of the nasal lumens and airway anatomy (including nasopharyngeal and trachea) during diagnostic procedures.

Source page: https://510kreport.com/device/K200740
Methodology: https://510kreport.com/methodology