# P000041: Rapidscreen RS-2000

- Pathway: PMA
- Applicant: Riverain Medical Group
- Decided: Jul 12, 2001 after 275 days
- Product code: MYN (Analyzer, Medical Image)
- Device class: 2
- Regulation: 21 CFR 892.2070
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
13 later devices descend from it; 2 cite it directly.
0 of 14 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. PMA decisions do not claim a predicate device.

## Most influential descendants
- K210666: Chest-CAD (2021), 8 descendants of its own
- K201560: Auto Lung Nodule Detection (2021), 3 descendants of its own
- K213353: Aorta-CAD (2022), 2 descendants of its own
- K241620: ChestView US (2025), 1 descendant of its own
- K230085: Lung-CAD (2023), 1 descendant of its own

Source page: https://510kreport.com/device/P000041
Methodology: https://510kreport.com/methodology