Clearance Summary
CorDx Tyfast COVID-19 Ag Rapid Test Rx received FDA 510(k) clearance under submission number K253882, sponsored by CorDx, Inc.. The device was reviewed via the Dual Track premarket notification pathway and assigned to the Microbiology review panel. The statutory decision date of record is 2026-06-01.
- Submission: K253882
- Applicant / Sponsor: CorDx, Inc.
- Clearance pathway: Dual Track
- Review panel: Microbiology
- Device class: Class II
- Regulation citation: 21 CFR 866.3982
- Decision date: 2026-06-01
Classification & Regulation
This clearance is catalogued under FDA product code QVF and 21 CFR 866.3982, within the Microbiology review panel as a Class II device.