EUA
BinaxNOW COVID-19 Antigen Self Test
FDA Emergency Use Authorization · Abbott Diagnostics Scarborough, Inc. · Nov 21, 2023
Key facts
| Product | BinaxNOW COVID-19 Antigen Self Test |
|---|---|
| Company | Abbott Diagnostics Scarborough, Inc. |
| Product type | Lateral Flow, Visual Read, Over the Counter (OTC) Home Testing, Serial Screening, Single Target |
| Date | Nov 21, 2023 |
| 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: