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Published 2 years ago

Seer Medical receives FDA 510(k) for its at-home epilepsy diagnosis aide

Summary by Ground News
Australian company Seer Medical received FDA 510(k) clearance for its at-home electroencephalograph (EEG) system. Seer Home enables patients to undergo week-long studies at home. The data collected is reviewed and annotated by a physician who then produces a report.

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Seer Medical receives FDA 510(k) for its at-home epilepsy diagnosis aide

The company’s Seer Home device allows for potential epilepsy diagnosis through at-home data collection.

2 years ago
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