Clearance Summary
iQ200 Series received FDA 510(k) clearance under submission number K252580, sponsored by Beckman Coulter, Inc.. The device was reviewed via the Special premarket notification pathway and assigned to the Hematology review panel. The statutory decision date of record is 2025-09-10.
- Submission: K252580
- Applicant / Sponsor: Beckman Coulter, Inc.
- Clearance pathway: Special
- Review panel: Hematology
- Device class: Class II
- Regulation citation: 21 CFR 864.5200
- Decision date: 2025-09-10
Classification & Regulation
This clearance is catalogued under FDA product code LKM and 21 CFR 864.5200, within the Hematology review panel as a Class II device.