# K933632: Medscan 12

- Pathway: 510(k) (Traditional)
- Applicant: Vidar Systems Corp.
- Decided: Dec 13, 1993 after 139 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
No predicates in its family tree.
8 later devices descend from it; 3 cite it directly.
0 of 9 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
- K993597: PLLL, Teleradpro, Model 12714/12715, VXR-12 Plus, Model 8619/9617 (1999), 4 descendants of its own
- K102476: Teleradpro (2010), 1 descendant of its own
- K993598: Mammography Pro, Model 13017, Diagnostic Pro W/ Mammography Option, Model 13205 (2000), 1 descendant of its own
- K130636: Teleradpro Edge; Teleradpro Edge HD-CCD (2013), 0 descendants of its own
- K130406: Diagnosticpro Edge (2013), 0 descendants of its own

Source page: https://510kreport.com/device/K933632
Methodology: https://510kreport.com/methodology