Clearance Summary
MULTIPLATE 5.0 AGGREGOMETER received FDA 510(k) clearance under submission number K103555, sponsored by Verum Diagnostica GmbH. The device was reviewed via the Traditional premarket notification pathway and assigned to the Hematology review panel. The statutory decision date of record is 2012-07-27.
- Submission: K103555
- Applicant / Sponsor: Verum Diagnostica GmbH
- Clearance pathway: Traditional
- Review panel: Hematology
- Device class: Class II
- Regulation citation: 21 CFR 864.5700
- Decision date: 2012-07-27
Classification & Regulation
This clearance is catalogued under FDA product code JOZ and 21 CFR 864.5700, within the Hematology review panel as a Class II device.