Carestart Covid-19 Antigen Home Test Kit In Singapore

For use under an Emergency Use Authorization (EUA) only for the duration of the COVID-19 declaration justifying the emergency use of in vitro diagnostics (IVD), unless it is terminated or revoked by the FDA (after which the test may no longer be used).
The AccessBio CareStart COVID-19 Antigen Test is only authorized for use in laboratories in the United States, certified under the Clinical Laboratory Improvement Amendments of 1988 (CLIA), CareStart Covid-19 Antigen Home Test Kit in Singapore 42 U.S.C. 263a, to perform high, moderate or waived complexity tests.
Please refer to the AccessBio CareStart COVID-19 Antigen Test instructions for use for additional information.