# K974493: Fiegert Endotech Flexible Fiberoptic Endoscopes, Fiegert Endotech Flexible Video-Endoscopes

- Pathway: 510(k) (Traditional)
- Applicant: Fiegert-Endotech Medizintechnik GmbH
- Decided: Mar 31, 1998 after 123 days
- Product code: FDS (Gastroscope 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.
No later device cites it as a predicate yet.
0 of 1 device in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. FDA’s file for it is a 510(k) statement, which names no predicate.

## Indications for use
Provide illumination to, and allow visual observation and/or surgical manipulation of body cavities, hollow organs and canals in the Gastrointestinal tract.

Source page: https://510kreport.com/device/K974493
Methodology: https://510kreport.com/methodology