Clearance Summary
ALPHA-THAL SCREEN 20 TEST KIT & 100 KIT received FDA 510(k) clearance under submission number K801771, sponsored by Isolab, 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 1981-01-16.
- Submission: K801771
- Applicant / Sponsor: Isolab, Inc.
- Clearance pathway: Traditional
- Review panel: Hematology
- Device class: Class II
- Regulation citation: 21 CFR 864.7500
- Decision date: 1981-01-16
Classification & Regulation
This clearance is catalogued under FDA product code LGL and 21 CFR 864.7500, within the Hematology review panel as a Class II device.