autoSCORE is an AI-enabled medical device from Holberg EEG AS, listed by FDA (510(k), K231068) with a decision date of 2024-01-07. Review panel: Neurology.
| FDA submission number | K231068 |
|---|---|
| Pathway | 510(k) |
| Company | Holberg EEG AS |
| Review panel (specialty) | Neurology |
| FDA decision date | 2024-01-07 |
| Decision | Substantially Equivalent |
| Product code | OMB |
| Classification | Automatic Event Detection Software For Full-Montage Electroencephalograph |
| Device class | 2 |
| Regulation number | 882.1400 |
| Review time (calendar days) | 268 |
| Applicant country | NO |
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Data from FDA's AI-enabled device list and openFDA. Informational only; verify against the FDA record.