Clearance Summary
BECKMAN DIATRAC HEMOGLOBIN A ELECTROPHORESIS KIT received FDA 510(k) clearance under submission number K905709, sponsored by Beckman Instruments, 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 1991-09-23.
- Submission: K905709
- Applicant / Sponsor: Beckman Instruments, Inc.
- Clearance pathway: Traditional
- Review panel: Hematology
- Device class: Class II
- Regulation citation: 21 CFR 864.7470
- Decision date: 1991-09-23
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.