Clearance Summary
Cytomics FC 500 Series (MPL or MCL) Flow Cytometer received FDA 510(k) clearance under submission number K182886, sponsored by Beckman Coulter. The device was reviewed via the Traditional premarket notification pathway and assigned to the Hematology review panel. The statutory decision date of record is 2019-09-06.
- Submission: K182886
- Applicant / Sponsor: Beckman Coulter
- Clearance pathway: Traditional
- Review panel: Hematology
- Device class: Class II
- Regulation citation: 21 CFR 864.5220
- Decision date: 2019-09-06
Classification & Regulation
This clearance is catalogued under FDA product code GKZ and 21 CFR 864.5220, within the Hematology review panel as a Class II device.