EUA
Maverick SARS-CoV-2 Multi-Antigen Serology Panel v2
FDA Emergency Use Authorization · Genalyte, Inc. · Oct 8, 2020
Key facts
| Product | Maverick SARS-CoV-2 Multi-Antigen Serology Panel v2 |
|---|---|
| Company | Genalyte, Inc. |
| Product type | Total Antibody, photonic ring immunoassay |
| Date | Oct 8, 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: