FDA Authorises First ML-Based COVID Screening Device

FDA has issued an emergency use authorisation for a Tiger Tech-released ML-based COVID-19 non-diagnostic screening device.

The US Food and Drug Administration (FDA) has issued an emergency use authorisation (EUA) for a Tiger Tech-released ML-based COVID-19 non-diagnostic screening device — COVID Plus Monitor. Termed to be first-of-its-kind, COVID Plus Monitor leverages machine learning that identifies certain biomarkers indicative of the virus that causes COVID-19.

Read more: https://analyticsindiamag.com/fda-authorises-first-ml-based-covid-screening-device/

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