Access Bio's newly developed blood-based IgG/IgM diagnostic test detects antibodiesproduced in response to infection by COVID-19. Access Bio’s standard test kit format received an Emergency Use Authorisation1 (EUA) by the US Food & Drug Administration(FDA) on 24 July 2020
Access Bio already have approval for their standard device but yet they are still wanting to uses Atomo's device so even if it was the same type of test there is still demand.
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