# K092739: Microendoscope Model S-0001 Single Light Source, Microendoscope, Model D-0001 Dual Light Source Sterile

- Pathway: 510(k) (Traditional)
- Applicant: C-Link Micro Imaging, Inc.
- Decided: Jan 12, 2010 after 126 days
- Product code: ODF (Mini Endoscope, Gastroenterology-Urology)
- Device class: 2
- Regulation: 21 CFR 876.1500
- 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 K011189 (2001). 1 ancestor in all.
No later device cites it as a predicate yet.
0 of 2 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K011189: Viaduct Microendoscope and Accessories, Acueity, Inc. (2001)

## Indications for use
This device is to be used by a physician for viewing an interior cavity of the human body through either a natural opening or an incision.

Source page: https://510kreport.com/device/K092739
Methodology: https://510kreport.com/methodology