# K081995: Stryker Vision Elect Whdtv (Stryker VE Whdtv)

- Pathway: 510(k) (Traditional)
- Applicant: Stryker Endoscopy
- Decided: Oct 2, 2008 after 80 days
- Product code: GCJ (Laparoscope, General & Plastic Surgery)
- 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.
9 later devices descend from it; 3 cite it directly.
0 of 10 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 its predicate without a number.
- (no number) Stryker Vision Elect HDTV: named in the summary without a submission number

## Most influential descendants
- K100195: NDS Surgical Imaging, LLC for the Zerowire Duo Wireless HD Video Transfer System, Model WU-WX-WY (Where U=R or T, W=P, X (2010), 7 descendants of its own
- K112621: WIS1000 (2012), 4 descendants of its own
- K151609: ZeroWire Duo Wireless HD Video Transfer System G2 or ZeroWire G2 (2015), 3 descendants of its own
- K161228: Radiance Ultra Series ZeroWire Embedded (2016), 2 descendants of its own
- K222890: Radiance Ultra 32 4K Zerowire Duo (2022), 0 descendants of its own

## Indications for use
The Stryker Vision Elect WHDTV (VE WHDTV) is intended for video display during surgical procedures including arthroscopy (orthopedic surgery), laparoscopy (general and gynecological surgery), thorascopy, endoscopy (general, gastroenterological and ENT surgery) and general surgery. The VE WHDTV is a non-sterile reusable device not intended for use in the sterile field. The VE WHDTV is intended for use by qualified physicians having complete knowledge of these surgical procedures.

Source page: https://510kreport.com/device/K081995
Methodology: https://510kreport.com/methodology