# K974315: Vidar VXR LS Laser Film Digitizer

- Pathway: 510(k) (Traditional)
- Applicant: Vidar Systems Corp.
- Decided: Apr 17, 1998 after 151 days
- Product code: LMA (Digitizer, Image, Radiological)
- Device class: 2
- Regulation: 21 CFR 892.2030
- 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 K934496 (1993). 1 ancestor in all.
2 later devices descend from it; 2 cite 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)
- K934496: X-Ray Angiographic System, Camtronics, Ltd. (1993) Summary page 1.

## Most influential descendants
- K992112: Samsung Raypax Film Digitizer (1999), 0 descendants of its own
- K984409: Elk Laser Film Digitizer (1999), 0 descendants of its own

## Indications for use
The Vidar VXR-LS Film Digitizer is intended for producing digital copies of medical x-ray films.

Source page: https://510kreport.com/device/K974315
Methodology: https://510kreport.com/methodology