Clearance Summary
GLYCOSAL HBA1C TEST received FDA 510(k) clearance under submission number K001392, sponsored by Provalis Diagnostics , Ltd.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Hematology review panel. The statutory decision date of record is 2000-08-21.
- Submission: K001392
- Applicant / Sponsor: Provalis Diagnostics , Ltd.
- Clearance pathway: Traditional
- Review panel: Hematology
- Device class: Class II
- Regulation citation: 21 CFR 864.7470
- Decision date: 2000-08-21
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.