510(k) K241313
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- May 30, 2025
- Date Received
- May 9, 2024
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Over-The-Counter Covid-19 Antigen Test
- Device Class
- Class II
- Regulation Number
- 866.3984
- Review Panel
- MI
- Submission Type
For the rapid, qualitative detection of SARS-CoV-2 virus nucleocapsid protein antigen in individuals 2 years and older.