# K940464: Karl Storz Uretero-Renoscope/Ureterscope

- Pathway: 510(k) (Traditional)
- Applicant: KARL STORZ Endoscopy-America, Inc.
- Decided: Jun 24, 1994 after 142 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
No predicates in its family tree.
5 later devices descend from it; 3 cite it directly.
0 of 6 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. FDA has not posted a summary or statement for it, so its predicates are not known.

## Most influential descendants
- K963855: 12 Ureteroscopes/Uretero-Renoscopes (1997), 2 descendants of its own
- K233372: KARL STORZ Fiber Telescopes for Urology (2024), 1 descendant of its own
- K253411: Miniature Telescope for Urology (27033AA) (2025), 0 descendants of its own
- K991178: Flexible Fiberscope, Model 7331.001, Guide Section for Lithovac Handpiece, Model 8708.253 (1999), 0 descendants of its own
- K990050: Uretero-Renoscope, Model 8706.402, Insertion Sheath, Model 8706.042 (1999), 0 descendants of its own

Source page: https://510kreport.com/device/K940464
Methodology: https://510kreport.com/methodology