Clearance Summary
FIBRI QUIK received FDA 510(k) clearance under submission number K802117, sponsored by General Diagnostics. The device was reviewed via the Traditional premarket notification pathway and assigned to the Hematology review panel. The statutory decision date of record is 1980-09-26.
- Submission: K802117
- Applicant / Sponsor: General Diagnostics
- Clearance pathway: Traditional
- Review panel: Hematology
- Device class: Class II
- Regulation citation: 21 CFR 864.7875
- Decision date: 1980-09-26
Classification & Regulation
This clearance is catalogued under FDA product code GJA and 21 CFR 864.7875, within the Hematology review panel as a Class II device.