Clearance Summary
POLLER CALIBRANTS received FDA 510(k) clearance under submission number K991439, sponsored by European Concerted Action on Anticoagulation. The device was reviewed via the Traditional premarket notification pathway and assigned to the Hematology review panel. The statutory decision date of record is 1999-12-20.
- Submission: K991439
- Applicant / Sponsor: European Concerted Action on Anticoagulation
- Clearance pathway: Traditional
- Review panel: Hematology
- Device class: Class II
- Regulation citation: 21 CFR 864.5425
- Decision date: 1999-12-20
Classification & Regulation
This clearance is catalogued under FDA product code GGN and 21 CFR 864.5425, within the Hematology review panel as a Class II device.