DM-Density is an AI-enabled medical device from Densitas, Inc., listed by FDA (510(k), K170540) with a decision date of 2018-02-23. Review panel: Radiology.
| FDA submission number | K170540 |
|---|---|
| Pathway | 510(k) |
| Company | Densitas, Inc. |
| Review panel (specialty) | Radiology |
| FDA decision date | 2018-02-23 |
| Decision | Substantially Equivalent |
| Product code | LLZ |
| Classification | System, Image Processing, Radiological |
| Device class | 2 |
| Regulation number | 892.2050 |
| Review time (calendar days) | 365 |
| Applicant country | CA |
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.