MR 5300 and MR 7700 R11 MR Systems is an AI-enabled medical device from Philips Medical Systems Nederlands B.V., listed by FDA (510(k), K223442) with a decision date of 2022-12-23. Review panel: Radiology.
| FDA submission number | K223442 |
|---|---|
| Pathway | 510(k) |
| Company | Philips Medical Systems Nederlands B.V. |
| Review panel (specialty) | Radiology |
| FDA decision date | 2022-12-23 |
| Decision | Substantially Equivalent |
| Product code | LNH |
| Classification | System, Nuclear Magnetic Resonance Imaging |
| Device class | 2 |
| Regulation number | 892.1000 |
| Review time (calendar days) | 39 |
| Applicant country | NL |
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.