RAPIDSCREEN RS-2000 is an AI-enabled medical device from RIVERAIN MEDICAL GROUP, listed by FDA (PMA, P000041) with a decision date of 2001-07-12. Review panel: Radiology.
| FDA submission number | P000041 |
|---|---|
| Pathway | PMA |
| Company | RIVERAIN MEDICAL GROUP |
| Review panel (specialty) | Radiology |
| FDA decision date | 2001-07-12 |
| Product code | MYN |
| Classification | Analyzer, Medical Image |
| Device class | 2 |
| Regulation number | 892.2070 |
| Review time (calendar days) | 275 |
Official FDA database record · FDA AI-enabled device list
All Radiology AI devices · Full device index
Data from FDA's AI-enabled device list and openFDA. Informational only; verify against the FDA record.