Corona-virus (COVID-19) IgM/IgG Rapid Test Kit, MADE IN USA- FDA APPROVAL PENDING
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Due to high demand, there is a 2 week lead time.
This product is for in vitro diagnostic use, following guidance from the FDA for Emergency Use Authorizations of tests submitted for approval on March 16, 2020. This test has not been reviewed by the FDA and results from antibody testing should not be used as the sole basis to diagnose or exclude SARS-CoV-2 (COVID-19) infection or to inform infection status.
In response to the COVID-19 pandemic and to help increase screening, RayBiotech is offering this rapid serology test to healthcare workers, hospitals, laboratories, and to other professionals only. This kit is not intended for at home use. If you feel you need to be tested, please reach out to a local clinic or physician and ask them about offering this test. Wash, Screen, Save!
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|IgM OR IgG:||
|Finger Prick Lancet Set:||
Without Lancet Set, With Lancet Set