# K993598: Mammography Pro, Model 13017, Diagnostic Pro W/ Mammography Option, Model 13205

- Pathway: 510(k) (Traditional)
- Applicant: Vidar Systems Corp.
- Decided: Jan 20, 2000 after 87 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.
1 later device descends from it; 1 cites it directly.
0 of 3 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
- K130406: Diagnosticpro Edge (2013), 0 descendants of its own

## Indications for use
The MAMMOGRAPHY PRO and Diagnostic PRO-M film digitizers are intended for converting analog Medical x-ray films to digital images. The devices are indicated for the digitization of mammography images for review and analysis, but not as the sole basis for screening or diagnosis.

Source page: https://510kreport.com/device/K993598
Methodology: https://510kreport.com/methodology