Description
Unit: 1 Box (25 Tests)
Regulatory Status: CLIA Waived/Professional Use Only
Contents: (25) Test devices + (2) extra for external QC, (25) extraction reagent capsules, (25) sterile swabs, (1) positive control swab, (1) negative control swab, (1) package insert with test procedure page
Sample Type: Nasal Swab
Storage Requirements: 59 F – 86 F
The OSOM Ultra Flu A&B Test is an in vitro rapid qualitative test that detects influenza type A and type B nucleoprotein antigens directly from a nasal swab obtained from patients with signs and symptoms of respiratory infection. OSOM Ultra Flu A&B Test was approved in November 2016 for CLIA Waiver status for nasal and nasopharyngeal swabs meeting the FDA performance criteria.