Clearance Summary
G7 AUTOMATED HPLC ANALYZER, BETA-THALASSEMIA MODE received FDA 510(k) clearance under submission number K020489, sponsored by Tosoh Medics, 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 2002-05-14.
- Submission: K020489
- Applicant / Sponsor: Tosoh Medics, Inc.
- Clearance pathway: Traditional
- Review panel: Hematology
- Device class: Class II
- Regulation citation: 21 CFR 864.7400
- Decision date: 2002-05-14
Classification & Regulation
This clearance is catalogued under FDA product code JPD and 21 CFR 864.7400, within the Hematology review panel as a Class II device.