Clearance Summary
BD Veritor System for Rapid Detection of Flu A+B CLIA Waived Kit received FDA 510(k) clearance under submission number K232434, sponsored by Bd. The device was reviewed via the Traditional premarket notification pathway and assigned to the Microbiology review panel. The statutory decision date of record is 2023-12-05.
- Submission: K232434
- Applicant / Sponsor: Bd
- Clearance pathway: Traditional
- Review panel: Microbiology
- Device class: Class II
- Regulation citation: 21 CFR 866.3328
- Decision date: 2023-12-05
Classification & Regulation
This clearance is catalogued under FDA product code PSZ and 21 CFR 866.3328, within the Microbiology review panel as a Class II device.