RAPIDSCREEN RS-2000 is an AI-enabled medical device from RIVERAIN MEDICAL GROUP that the U.S. FDA approved through PMA P000041 on July 12, 2001. Its lead review panel is Radiology and its primary product code is MYN.
See also top radiology AI devices.
Key facts
| Submission number | P000041 |
|---|---|
| Pathway | PMA |
| Date of final decision | |
| Company (FDA list) | RIVERAIN MEDICAL GROUP |
| Lead review panel | Radiology |
| Primary product code | MYN |
Source: FDA AI-Enabled Medical Devices list. No matching openFDA record was found for this submission yet.
What this means
Premarket Approval (PMA) is FDA's most stringent pathway, used for Class III devices. It requires valid scientific evidence of safety and effectiveness. RAPIDSCREEN RS-2000 went through this pathway (P000041).
Product code MYN covers 43 devices on the FDA AI list. By decision date, this device is #3 of 43 under that code. RIVERAIN MEDICAL GROUP has 1 AI-enabled device on the list, and the Radiology panel accounts for 1,230 in total.
Being on this list doesn't describe how well the device works clinically. Check the FDA record for its indications for use.