EUA
Status COVID-19 Antigen Rapid Test for Home Use
FDA Emergency Use Authorization · Princeton BioMeditech Corp. · Jun 28, 2023
Key facts
| Product | Status COVID-19 Antigen Rapid Test for Home Use |
|---|---|
| Company | Princeton BioMeditech Corp. |
| Product type | Lateral Flow, Visual Read, Over the Counter (OTC) Home Testing, Serial Screening, Single Target |
| Date | Jun 28, 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: