# K170930: RSM 2430C

- Pathway: 510(k) (Special)
- Applicant: DRTECH Corporation
- Decided: Apr 27, 2017 after 29 days
- Product code: MUE (Full Field Digital, System, X-Ray, Mammographic)
- Device class: 2
- Regulation: 21 CFR 892.1715
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 10 generations back to K896095 (1990). 13 ancestors in all.
1 later device descends from it; 1 cites it directly.
0 of 15 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K162670: RSM 1824C with RConsole1, DRTECH Corporation (2017) Summary page 4.

## Most influential descendants
- K241113: Vivix-M (2025), 0 descendants of its own

## Indications for use
The RSM 2430C is a detector indicated for use in screening and diagnostic mammography.

Source page: https://510kreport.com/device/K170930
Methodology: https://510kreport.com/methodology