# K203226: Telescope 0 O 10MM WL 305MM / Telescope 30 O 10MM WL 305MM / Telescope 50 O 10MM WL 305MM, Telescope 0 O 10MM WL 440MM / Telescope 30 O 10MM WL 440MM / Telescope 50 O 10MM WL 440MM

- Pathway: 510(k) (Traditional)
- Applicant: Richard Wolf Medical Instruments Corporation
- Decided: May 14, 2021 after 193 days
- Product code: GCM (Endoscope, 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: 1 generation back to K993103 (1999). 1 ancestor in all.
2 later devices descend from it; 2 cite it directly.
0 of 4 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K993103: Endoscopes,10MM Diameter 0 Degrees; Endoscopes, 10MM Diameter, 30 Degrees; Endoscopes, 10MM Diameter, 50 Degrees, Richard Wolf Medical Instruments Corp. (1999) Summary page 5.

## Most influential descendants
- K260414: “Tech-Image” Video Endoscope System (2026), 0 descendants of its own
- K212808: Logic Hd camera head green, System green (2022), 0 descendants of its own

## Indications for use
The products are used in invasive surgery or via natural orifices for diagnosis and therapy and serve to visualize the inside of the body. The products are used for interventions in different medical disciplines, such as surgery and laparoscopic interventions e.g. in urology and gynecology.

Source page: https://510kreport.com/device/K203226
Methodology: https://510kreport.com/methodology