# K934496: X-Ray Angiographic System

- Pathway: 510(k) (Traditional)
- Applicant: Camtronics, Ltd.
- Decided: Dec 13, 1993 after 89 days
- Product code: IZI (System, X-Ray, Angiographic)
- Device class: 2
- Regulation: 21 CFR 892.1600
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
6 later devices descend from it; 3 cite it directly.
0 of 7 devices 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.

## Most influential descendants
- K974315: Vidar VXR LS Laser Film Digitizer (1998), 2 descendants of its own
- K955519: Analytical Review Station (1996), 1 descendant of its own
- K992073: AX Workstation (1999), 0 descendants of its own
- K992112: Samsung Raypax Film Digitizer (1999), 0 descendants of its own
- K984409: Elk Laser Film Digitizer (1999), 0 descendants of its own

Source page: https://510kreport.com/device/K934496
Methodology: https://510kreport.com/methodology