Clearance Summary
Access Rubella IgG received FDA 510(k) clearance under submission number K250588, sponsored by Beckman Coulter, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Microbiology review panel. The statutory decision date of record is 2025-11-17.
- Submission: K250588
- Applicant / Sponsor: Beckman Coulter, Inc.
- Clearance pathway: Traditional
- Review panel: Microbiology
- Device class: Class II
- Regulation citation: 21 CFR 866.3510
- Decision date: 2025-11-17
Classification & Regulation
This clearance is catalogued under FDA product code LFX and 21 CFR 866.3510, within the Microbiology review panel as a Class II device.