# K993597: PLLL, Teleradpro, Model 12714/12715, VXR-12 Plus, Model 8619/9617

- Pathway: 510(k) (Traditional)
- Applicant: Vidar Systems Corp.
- Decided: Dec 15, 1999 after 51 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.
4 later devices descend from it; 3 cite it directly.
0 of 6 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.

## Most influential descendants
- K102476: Teleradpro (2010), 1 descendant of its own
- K130636: Teleradpro Edge; Teleradpro Edge HD-CCD (2013), 0 descendants of its own
- K093809: Vidar Dental Film Digitizer (2010), 0 descendants of its own
- K091288: Medi-6000 Medical Image Digitizer (2009), 0 descendants of its own

## Indications for use
The VIDAR P 111, TeleRADPRO, and VXR-12 plus film digitizers are intended for making digital copies of medical x-ray films.

Source page: https://510kreport.com/device/K993597
Methodology: https://510kreport.com/methodology