Clearance Summary
A1C 2.2 PLUS - AUTOMATED GLYCOHEMOGLOBIN ANALYZER received FDA 510(k) clearance under submission number K972265, 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 1997-09-25.
- Submission: K972265
- Applicant / Sponsor: Tosoh Medics, Inc.
- Clearance pathway: Traditional
- Review panel: Hematology
- Device class: Class II
- Regulation citation: 21 CFR 864.7470
- Decision date: 1997-09-25
Classification & Regulation
This clearance is catalogued under FDA product code LCP and 21 CFR 864.7470, within the Hematology review panel as a Class II device.