# K082451: Stryker Videoscope

- Pathway: 510(k) (Traditional)
- Applicant: Stryker Endoscopy
- Decided: Dec 16, 2008 after 113 days
- Product code: HET (Laparoscope, Gynecologic (And Accessories))
- Device class: 2
- Regulation: 21 CFR 884.1720
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 3 generations back to K923982 (1993). 7 ancestors in all.
No later device cites it as a predicate yet.
0 of 8 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K053382: Laparo-Thoraco Videoscope XLTF-Vaw, Olympus Medical Systems Corporation (2006) Summary page 1.

## Indications for use
The Stryker Videoscope is a video endoscope indicated for use in endoscopy and endoscopic surgery within the thoracic and abdominal cavities, including female reproductive organs.

Source page: https://510kreport.com/device/K082451
Methodology: https://510kreport.com/methodology