Clearance Summary
IQ 200 SYSTEM received FDA 510(k) clearance under submission number K022774, sponsored by Intl. Remote Imaging Systems. The device was reviewed via the Traditional premarket notification pathway and assigned to the Hematology review panel. The statutory decision date of record is 2002-10-21.
- Submission: K022774
- Applicant / Sponsor: Intl. Remote Imaging Systems
- Clearance pathway: Traditional
- Review panel: Hematology
- Device class: Class II
- Regulation citation: 21 CFR 864.5200
- Decision date: 2002-10-21
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.