Clearance Summary
COAGULATOR (8 CHANNEL) received FDA 510(k) clearance under submission number K862047, sponsored by Med USA. The device was reviewed via the Traditional premarket notification pathway and assigned to the Hematology review panel. The statutory decision date of record is 1986-09-29.
- Submission: K862047
- Applicant / Sponsor: Med USA
- Clearance pathway: Traditional
- Review panel: Hematology
- Device class: Class II
- Regulation citation: 21 CFR 864.5400
- Decision date: 1986-09-29
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.