# K242779: Hood (DH-083ST)

- Pathway: 510(k) (Special)
- Applicant: Fujifilm Corporation
- Decided: Oct 11, 2024 after 28 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
Longest line of descent: 6 generations back to K993704 (2000). 9 ancestors in all.
No later device cites it as a predicate yet.
0 of 10 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K232314: Hood (DH-106STL, DH-116STL, DH-126STL, DH-096ST), FUJIFILM Healthcare Americas Corporation (2023) Summary page 5.

## Indications for use
This hood is intended to be used in combination with compatible endoscopes to maintain the field of view during endoscopic procedures such as mucosal resection.

Source page: https://510kreport.com/device/K242779
Methodology: https://510kreport.com/methodology