Clearance Summary
Accula Strep A Test received FDA 510(k) clearance under submission number K201269, sponsored by Mesa Biotech, 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 2020-11-09.
- Submission: K201269
- Applicant / Sponsor: Mesa Biotech, Inc.
- Clearance pathway: Dual Track
- Review panel: Microbiology
- Device class: Class II
- Regulation citation: 21 CFR 866.2680
- Decision date: 2020-11-09
Classification & Regulation
This clearance is catalogued under FDA product code PGX and 21 CFR 866.2680, within the Microbiology review panel as a Class II device.