DUNE MEDICAL DEVICES MARGINPROBE SYSTEM is an AI-enabled medical device from Dilon Medical Technologies, Ltd., listed by FDA (PMA, P110014) with a decision date of 2012-12-27. Review panel: General and Plastic Surgery.
| FDA submission number | P110014 |
|---|---|
| Pathway | PMA |
| Company | Dilon Medical Technologies, Ltd. |
| Review panel (specialty) | General and Plastic Surgery |
| FDA decision date | 2012-12-27 |
| Product code | OEE |
| Classification | Diagnostic Low Electric Field |
| Device class | 3 |
| Review time (calendar days) | 633 |
Official FDA database record · FDA AI-enabled device list
All General and Plastic Surgery AI devices · Full device index
Data from FDA's AI-enabled device list and openFDA. Informational only; verify against the FDA record.