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COVID-19 Rapid
Antigen Test

FDA-EUA Authorized

  • Fast & Easy, HCP Assisted
  • Results in as Little as 10 minutes
  • Symptomatic & Asymptomatic Testing
  • Requires Training
20 tests per box
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How It Works

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Step 1: Order Test Kits

Use the form above to order kits and your test kits will be delivered promptly.

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Step 2: Complete Antigen Test Training

Undergo antigen test training prior to administering tests.

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Step 3: Collect Patient’s Samples

The trained test administrator will collect samples from patients in accordance with your testing policy.

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Step 4: Receive Patient’s Results

Once the sample has been inserted into the testing device, results will be displayed in 10 minutes.

FDA Emergency Use Authorized
COVID-19 Rapid Antigen Test

Our rapid point-of-care testing kit for COVID-19 uses a nasopharyngeal swab to determine if your employees are infected with the SARS-CoV-2 virus. This test is offered under the Emergency Use Authorization guidelines issued by the FDA. Each box contains everything you need to perform 20 rapid antigen tests. Results will be displayed on the testing device 10 minutes after the sample is inserted.

Collection Method:
Nasopharyngeal Swab

Collection Method:
Nasopharyngeal Swab

Results Displayed on Device In:
10 minutes

FDA Emergency Use Authorization
https://www.fda.gov/media/142916/download

FDA Authorization

This test has been authorized by the FDA under an Emergency Use Authorization for use by authorized laboratories. This test has not been FDA cleared or approved. This test has been authorized only for the detection of nucleic acid from SARS-CoV-2, not for any other viruses or pathogens. This test is only authorized for the duration of the declaration that circumstances exist justifying the authorization of emergency use of in vitro diagnostic tests for detection and/or diagnosis of COVID-19 under Section 564(b)(1) of the Act, 21 U.S.C. § 360bbb-3(b)(1), unless the authorization is terminated or revoked sooner.