# K935234: Stryker Endoscopic Video Accessories

- Pathway: 510(k) (Traditional)
- Applicant: Stryker Endoscopy
- Decided: Mar 18, 1994 after 137 days
- Product code: GCJ (Laparoscope, General & Plastic Surgery)
- Device class: 2
- Regulation: 21 CFR 876.1500
- Recalls of this device: 3 (0 Class I)
- 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 has not posted a summary or statement for it, so its predicates are not known.

## Recalls of this device
- Apr 16, 2010 · Not classified · Z-0922-2011: The electrical cord power plug design may allow the prongs to develop a fracture inside or outside the plug, if the plug is misused.
- Sep 22, 2008 · Not classified · Z-0196-2009: Knob parts stick together, resulting in poor functionality of the knob.
- Nov 30, 2004 · Not classified · Z-0417-05: A problem with the design of the transformers may cause the transformers' circuit breakers to trip, which could result in loss of power to connected medical devices.

Source page: https://510kreport.com/device/K935234
Methodology: https://510kreport.com/methodology