FDA approved Rapid Covid Antigen tests from a US company. CLIA-waived.
• The Sienna-Clarity COVID-19 Antigen test can be
used to test directly collected nasopharyngeal swab
specimens.
• The Sienna-Clarity COVID-19 Antigen test should be
ordered for the detection of COVID-19 antigen in
individuals who are suspected of COVID-19 by their
healthcare provider and who are within six days of
symptom onset.
• The Sienna-Clarity COVID-19 Antigen test is
authorized for use in laboratories certified under the
Clinical Laboratory Improvement Amendments of
1988 (CLIA), 42 U.S.C. §263a, that meet
requirements to perform high complexity, moderate
complexity, or waived tests. This test is authorized
for use at the Point of Care (POC), i.e., patient care
settings operating under a CLIA Certificate of
Waiver, Certificate of Compliance, or Certificate of
Accreditation.
CLICK HERE to DOWNLOAD FDA STATEMENT
Clarity COVID-19 Antigen Rapid Test Kits, Includes: (25) Tests, (25) NP Swabs, (25) Buffers, Package Insert, QSG, (1) Negative Control, and (1) Positive Control/kt
25 tests per box. Priced by the box.