# K993103: Endoscopes,10MM Diameter 0 Degrees; Endoscopes, 10MM Diameter, 30 Degrees; Endoscopes, 10MM Diameter, 50 Degrees

- Pathway: 510(k) (Traditional)
- Applicant: Richard Wolf Medical Instruments Corp.
- Decided: Dec 10, 1999 after 85 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
No predicates in its family tree.
3 later devices descend from it; 1 cites 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)
- None. The FDA summary names no predicate by number.

## Most influential descendants
- 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 (2021), 2 descendants of its own
- 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 endoscopes serve to visualize the inside of the patient via natural or surgically generated access. For examination, diagnosis, and / or therapy by personnel trained and qualified in connection with endoscopically used aczessories in various medical disciplines, such as surgery, urology, gynecology, and ENT.

Source page: https://510kreport.com/device/K993103
Methodology: https://510kreport.com/methodology