The primary objective of this study is device feasibility of the Diassess Influenza A and B Test
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
DEVICE_FEASIBILITY
Masking
NONE
Enrollment
567
University Health Care Center
Syracuse, New York, United States
Diassess test measurement agreement with Polymerase Chain Reaction (PCR)
Time frame: One (1) patient visit which is a time frame of one (1) hour
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