Clearance Summary
SYSMEX MODEL XT-4000I received FDA 510(k) clearance under submission number K091313, sponsored by Sysmex America, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Hematology review panel. The statutory decision date of record is 2010-03-30.
- Submission: K091313
- Applicant / Sponsor: Sysmex America, Inc.
- Clearance pathway: Traditional
- Review panel: Hematology
- Device class: Class II
- Regulation citation: 21 CFR 864.5220
- Decision date: 2010-03-30
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.