# K992666: Video Plus System, Series 95000

- Pathway: 510(k) (Traditional)
- Applicant: Camtronics, Ltd.
- Decided: Oct 13, 1999 after 65 days
- Product code: LLZ (System, Image Processing, Radiological)
- Device class: 2
- Regulation: 21 CFR 892.2050
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 1 generation back to K926258 (1993). 2 ancestors in all.
1 later device descends from it; 1 cites it directly.
0 of 4 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K945459: DLX, General Electric Co. (1995) Summary page 1.
- K926258: DLX, GE Medical Systems (1993) Summary page 1.

## Most influential descendants
- K031638: Cardio Vascular Information Enhanced Workstation (2003), 0 descendants of its own

## Indications for use
Video Plus is a digital imaging acquisition and review system for the cardiac catheterization lab. Its features include digital fluoroscopy, digital cine, real time processing during acquisition, DSA processing, image processing, quantitative coronary analysis, digital subtraction angiography, digital video input, linked biplane acquisition, auto injection, and histogram equalization.

Source page: https://510kreport.com/device/K992666
Methodology: https://510kreport.com/methodology