Clearance Summary
Xpert Xpress MVP, GeneXpert Dx System, GeneXpert Infinity System received FDA 510(k) clearance under submission number K221160, sponsored by Cepheid. The device was reviewed via the Special premarket notification pathway and assigned to the Microbiology review panel. The statutory decision date of record is 2022-06-07.
- Submission: K221160
- Applicant / Sponsor: Cepheid
- Clearance pathway: Special
- Review panel: Microbiology
- Device class: Class II
- Regulation citation: 21 CFR 866.3975
- Decision date: 2022-06-07
Classification & Regulation
This clearance is catalogued under FDA product code PQA and 21 CFR 866.3975, within the Microbiology review panel as a Class II device.