Clearance Summary
ACL TOP FAMILY 50 SERIES: ACL TOP 350 CTS; ACL TOP 550 CTS; ACL TOP 750; ACL TOP 750 CTS; ACL TOP 750 LAS received FDA 510(k) clearance under submission number K150877, sponsored by Instrumentation Laboratory CO. The device was reviewed via the Traditional premarket notification pathway and assigned to the Hematology review panel. The statutory decision date of record is 2015-12-13.
- Submission: K150877
- Applicant / Sponsor: Instrumentation Laboratory CO
- Clearance pathway: Traditional
- Review panel: Hematology
- Device class: Class II
- Regulation citation: 21 CFR 864.5400
- Decision date: 2015-12-13
Classification & Regulation
This clearance is catalogued under FDA product code GKP and 21 CFR 864.5400, within the Hematology review panel as a Class II device.