Monday, November 1, 2021

FDA Authorizes Additional Indication for OTC COVID-19 Test

The OraSure Technologies InteliSwab COVID-19 Rapid Test can be used without a prescription; gives results in 30 minutes.

If your email program has trouble displaying this email, view as a webpage.

FDA - Center for Devices and Radiological Health

Bookmark and Share

FDA Authorizes Additional Indication for OraSure InteliSwab COVID-19 Over-the-Counter Antigen Test

The U.S. Food and Drug Administration (FDA) reissued the emergency use authorization (EUA) for the OraSure Technologies InteliSwab COVID-19 Rapid Test.

The InteliSwab COVID-19 Rapid Test gives results in 30 minutes and can be used:

  • Without a prescription.
  • As a single test for people with COVID-19 symptoms.
  • As a serial test for people without COVID-19 symptoms, meaning the test must be done twice over three days.
  • For people 18 years of age and older with a self-collected nasal swab sample or people 15 years of age and older when an adult collects the nasal swab sample.

The FDA reissued the EUA to authorize use of InteliSwab COVID-19 Rapid Test as a single test without a prescription for people with COVID-19 symptoms. The test was already authorized for use as a serial test without a prescription by people with or without COVID-19 symptoms and as a single use test with a prescription for symptomatic people who are suspected of COVID-19 by their healthcare provider.

The FDA is committed to increasing the availability of accurate and reliable at-home COVID-19 diagnostic tests, and to facilitating consumer access to these tests.

Questions?

If you have questions about OTC COVID-19 tests, contact the Division of Industry and Consumer Education 


This email was sent to ooseims.archieves@blogger.com using GovDelivery Communications Cloud on behalf of: U.S. Food and Drug Administration · 
10903 New Hampshire Ave · Silver Spring, MD ·  20993-0002 ·  1-888-INFO-FDA
GovDelivery logo

No comments:

Post a Comment