# K190190: WV1 Endoscope

- Pathway: 510(k) (Traditional)
- Applicant: 270surgical, Ltd.
- Decided: Nov 1, 2019 after 273 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: 2 generations back to K955456 (1996). 3 ancestors in all.
1 later device descends from it; 1 cites it directly.
0 of 5 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K111788: Endoeye HD II, Olympus America, Inc. (2012) Summary page 4.

## Most influential descendants
- K210104: SurroundScope System (2021), 0 descendants of its own

## Indications for use
The WV1 endoscope is a reusable, rigid, video endoscope, designed to be used with a video system center, light source, documentation equipment, monitor, hand instruments, electrosurgical unit, and other ancillary equipment for endoscopy and endoscopic surgery within the thoracic and abdominal cavities including the female reproductive organs.

Source page: https://510kreport.com/device/K190190
Methodology: https://510kreport.com/methodology