# K993599: Diagnostic Pro, Model 12772, VXR-16, Model 13020, VXR-16 Dosimetry Pro, Model 13019

- Pathway: 510(k) (Traditional)
- Applicant: Vidar Systems Corp.
- Decided: Jan 18, 2000 after 85 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 K933632 (1993). 1 ancestor in all.
No later device cites it as a predicate yet.
0 of 2 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K933632: Medscan 12, Vidar Systems Corp. (1993) Summary page 1.

## Indications for use
The Diagnostic PRO, VXR-16, and VXR-16 DOSIMETRYPRO film digitizers are intended for making digital copies of medical x-ray films.

Source page: https://510kreport.com/device/K993599
Methodology: https://510kreport.com/methodology