Clearance Summary
FIBRON-1, FIBRON-4, QUIKCOAG, FIBRON received FDA 510(k) clearance under submission number K021976, sponsored by Vital Scientific N.V.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Hematology review panel. The statutory decision date of record is 2002-10-25.
- Submission: K021976
- Applicant / Sponsor: Vital Scientific N.V.
- Clearance pathway: Traditional
- Review panel: Hematology
- Device class: Class II
- Regulation citation: 21 CFR 864.5400
- Decision date: 2002-10-25
Classification & Regulation
This clearance is catalogued under FDA product code KQG and 21 CFR 864.5400, within the Hematology review panel as a Class II device.