The document summarizes Florida's emergency rule allowing students to shorten quarantine or isolation periods if they test negative for COVID-19. It lists FDA-authorized antigen and molecular COVID tests, indicating whether they are over-the-counter, prescription, or for home/at-home use for symptomatic or asymptomatic individuals. The tests approved for shortening quarantine include antigen tests used as directed and any PCR test processed by a lab.
The document summarizes Florida's emergency rule allowing students to shorten quarantine or isolation periods if they test negative for COVID-19. It lists FDA-authorized antigen and molecular COVID tests, indicating whether they are over-the-counter, prescription, or for home/at-home use for symptomatic or asymptomatic individuals. The tests approved for shortening quarantine include antigen tests used as directed and any PCR test processed by a lab.
The document summarizes Florida's emergency rule allowing students to shorten quarantine or isolation periods if they test negative for COVID-19. It lists FDA-authorized antigen and molecular COVID tests, indicating whether they are over-the-counter, prescription, or for home/at-home use for symptomatic or asymptomatic individuals. The tests approved for shortening quarantine include antigen tests used as directed and any PCR test processed by a lab.
The document summarizes Florida's emergency rule allowing students to shorten quarantine or isolation periods if they test negative for COVID-19. It lists FDA-authorized antigen and molecular COVID tests, indicating whether they are over-the-counter, prescription, or for home/at-home use for symptomatic or asymptomatic individuals. The tests approved for shortening quarantine include antigen tests used as directed and any PCR test processed by a lab.
Florida Department of Health Emergency Rule 64DER21-12 provides opportunities for public school students to reduce quarantine or
isolation if they are asymptomatic and receive a negative diagnostic test for COVID-19.1 If a public school student is using one of the opportunities, as described in Emergency Rule 64DER21-12, to obtain a diagnostic COVID-19 test result to shorten their isolation or quarantine period, the COVID-19 diagnostic test should have received Emergency Use Authorization (EUA) from, or full approval by, the Food and Drug Administration (FDA) and the COVID-19 test should be used in the same manner specified by FDA’s authorization or approval. The table below lists current COVID-19 diagnostic tests that have received an EUA by the FDA and how they can (i.e., over the counter or at-home) and should (i.e., symptomatic and/or asymptomatic) be used. COVID-19 Tests that have received EUA from the FDA 2 Antigen Tests Symptomatic Asymptomatic Over the Counter Tests Prescription At-Home Use Use3 Tests Ellume COVID-19 Home Test X X X BinaxNOW COVID-19 Ag Card 2 Home Test X X QuickVue At-Home OTC COVID-19 Test X X BinaxNOW COVID-19 Antigen Self Test X X InteliSwab COVID-19 Rapid Test X X CareStart COVID-19 Antigen Home Test X X InteliSwab COVID-19 Rapid Test Rx X X BinaxNOW COVID-19 Ag Card Home Test X X QuickVue At-Home COVID-19 Test X X InteliSwab COVID-19 Rapid Test Pro X BinaxNOW COVID-19 Ag Card X BinaxNOW COVID-19 Ag 2 Card X CareStart COVID-19 Antigen X BD Veritor System for Rapid Detection of X SARS-CoV-2 BD Veritor System for Rapid Detection of X SARS-CoV-2 & Flu A&B Sampinute COVID-19 Antigen MIA X LIAISON SARS-CoV-2 Ag X
1 https://www.flgov.com/wp-content/uploads/2021/08/8.6.21-DOH-Rule.pdf 2 https://www.fda.gov/medical-devices/coronavirus-disease-2019-covid-19-emergency-use-authorizations-medical-devices/in-vitro-diagnostics-euas-antigen-diagnostic-tests-sars-cov-2 3 These tests have been approved for “Screening” and can be used for asymptomatic testing; this is not to be confused with “Serial Screening.”
August 19, 2021 1
ellume.lab COVID Antigen Test X GenBody COVID-19 Ag X SCoV-2 Ag Detect Rapid Test X CLIP COVID Rapid Antigen Test X LumiraDX SARS-CoV-2 Ag Test X VITROS Immunodiagnostic Products X INDICAID COVID-19 Rapid Antigen Test X Status COVID-10/Flu X QIAreach SARS-CoV-2 Antigen X Omnia SARS-CoV-2 Antigen Test X Simoa SARS-CoV-2 N Protein Antigen Test X Sofia SARS Antigen FIA X Sofia 2 Flu + SARS Antigen FIA X QuickVue SARS Antigen Test X Sienna-Clarify COVID-19 Antigen Test Rapid X Test Cassette
Molecular Tests4 Any PCR Test given by provider or sent to a X X commercial laboratory5 Lucira CHECK-IT COVID-19 Test Kit X X X Cue COVID-19 Test for Home and Over the X X X Counter (OTC) Use Lucira COVID-19 All-In-One Test Kit X X X Everly COVID-19 Test Home Collection Kit X X X Direct to Consumer Kroger Health COVID-19 Test Home Collection X X X Kit Color COVID-19 Self-Swab Collection Kit X X X
4 https://www.fda.gov/medical-devices/coronavirus-disease-2019-covid-19-emergency-use-authorizations-medical-devices/in-vitro-diagnostics-euas-molecular-diagnostic-tests-sars- cov-2 5 Includes “Direct to Consumer” and “Home Collection” tests, as these tests are sent to a commercial laboratory.
August 19, 2021 2
EmpowerDX COVID-19 Home Collection Kit X X X Direct to Consumer binx health At-Home Nasal Swab Collection Kit X X X GetMyDNA COVID-19 Test Home Collection X X X Kit Pinpoint by Phosphorus COVID-19 Test Home X X X Collection Kit DTC WREN Laboratories COVID-19 Saliva Test X X X Collection Kit DTC
