Clearance Summary
IL SYSTEM 810, ACL AND THE REAGENT SETS received FDA 510(k) clearance under submission number K862301, 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 1986-09-03.
- Submission: K862301
- Applicant / Sponsor: Instrumentation Laboratory CO
- Clearance pathway: Traditional
- Review panel: Hematology
- Device class: Class II
- Regulation citation: 21 CFR 864.7875
- Decision date: 1986-09-03
Classification & Regulation
This clearance is catalogued under FDA product code GJA and 21 CFR 864.7875, within the Hematology review panel as a Class II device.