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Description
Description
- The Fastep COVID-19 Antigen Pen Home Test is for FDA Emergency Use Authorization (EUA) only: https://www.fda.gov/medical-devices/covid-19-emergency-use-authorizations-medical-devices/in-vitro-diagnostics-euas-antigen-diagnostic-tests-sars-cov-2
- Fastep COVID-19 Antigen Pen Home Test is a lateral flow immunoassay device intended for the qualitative detection of nucleocapsid protein antigen from the SARS-CoV-2 virus
- This test is authorized for non-prescription home use with self-collected anterior nasal (nares) swab samples from individuals aged 14 years or older or adult collected anterior nasal (nares) swab samples from individuals aged two (2) years or older
- This test is authorized for individuals with symptoms of COVID-19 within the first 6 days of symptom onset when tested at least twice over three days with at least 48 hours between tests, and for individuals without symptoms or other epidemiological reasons to suspect COVID-19, when tested at least three times over five days with at least 48 hours between tests
- Positive results indicate the presence of viral antigens, but clinical correlation with past medical history and other diagnostic information is necessary to determine infection status; positive results do not rule out bacterial infection or co-infection with other viruses
- All negative results are presumptive and confirmation with a molecular assay, if necessary for patient management, may be performed
- Negative results do not rule out SARS-CoV-2 infection and should not be used as the sole basis for treatment or patient management decisions, including infection control measures such as isolating from others and wearing masks; negative results should be considered in the context of an individual’s recent exposures, history, and the presence of clinical signs and symptoms consistent with COVID-19
- All healthcare providers will report all test results they receive from individuals who use the authorized product to relevant public health authorities in accordance with local, state, and federal requirements using appropriate LOINC and SNOMED codes, as defined by the Laboratory In Vitro Diagnostics (LIVD) Test Code Mapping for SARS-CoV-2 Tests provided by CDC
- The Fastep® COVID-19 Antigen Pen Home Test is a single test comprised of a base and a test pen with an integrated sample swab and test strip
- Each Fastep® COVID-19 Antigen Pen Home Test has a built-in internal procedural control
Specifications
Specifications
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Product Document(s)
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ApplicationRespiratory Test Kit
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Contents 1Each Kit contains (1) Foil Package with Base and Test Pen, (1) Package Insert
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Number of Tests1 Test per Kit (144 Kits per Case)
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Purchase Program TypeStandard Purchase
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Reading TypeVisual Read
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Sample TypeAnterior Nasal (Nares) Swab Sample
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SpecialtyImmunoassay
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Test FormatTest Device Format
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Test Kit TypeRapid
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Test MethodLateral Flow
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Test NameCOVID-19 Antigen Pen Test
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Test TypeHome Test Device
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Time to Results15 Minute Results
FaStep COVID-19 Antigen Pen Home Test FDA EUA Letter
FaStep COVID-19 Antigen Pen Home Test IFU
FaStep COVID-19 Antigen Pen Home Test Healthcare Professionals Fact Sheet
FaStep COVID-19 Antigen Pen Home Test Quick Ref Guide
Return policy
Return policy
Not loving it? We offer returns for most items within 30 days of delivery for a refund or store credit.
