EUA
RightSign COVID-19 IgG/IgM Rapid Test Cassette
FDA Emergency Use Authorization · Hangzhou Biotest Biotech Co., Ltd. · Dec 21, 2020
Key facts
| Product | RightSign COVID-19 IgG/IgM Rapid Test Cassette |
|---|---|
| Company | Hangzhou Biotest Biotech Co., Ltd. |
| Product type | IgM and IgG Lateral Flow, Fingerstick Whole Blood |
| Date | Dec 21, 2020 |
| FDA page | fda.gov |
At a glance
- 1–9 Authorization documents
- 1–9 EUAs for this company
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About Emergency Use Authorizations
Emergency Use Authorizations allow the FDA to permit unapproved medical products, or unapproved uses of approved products, during a declared public health emergency.
Source: U.S. Food and Drug Administration (FDA), Emergency Use Authorizations · Source date: