# K121112: Stryker Video Ureteroscope

- Pathway: 510(k) (Traditional)
- Applicant: Stryker Endoscopy
- Decided: Sep 12, 2012 after 153 days
- Product code: FGB (Ureteroscope And Accessories, Flexible/Rigid)
- 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: 2 generations back to K951855 (1995). 2 ancestors in all.
No later device cites it as a predicate yet.
0 of 3 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K033651: Olympus Video Ureteroscope, NTSC, Olympus Winter & Ibe GmbH (2004) Summary page 1.

## Indications for use
The Stryker Video Ureteroscope is designed to be used with a Stryker video system, monitor and other accessories for endoscopic diagnosis and treatment within the urethra, bladder, ureter, and kidney.

Source page: https://510kreport.com/device/K121112
Methodology: https://510kreport.com/methodology