Clearance Summary
ADDITIONAL HEMOTEC ACT COAGULATION CARTRIDGES received FDA 510(k) clearance under submission number K853198, sponsored by Medical Device Consultants, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Hematology review panel. The statutory decision date of record is 1985-10-04.
- Submission: K853198
- Applicant / Sponsor: Medical Device Consultants, Inc.
- Clearance pathway: Traditional
- Review panel: Hematology
- Device class: Class II
- Regulation citation: 21 CFR 864.5425
- Decision date: 1985-10-04
Classification & Regulation
This clearance is catalogued under FDA product code JPA and 21 CFR 864.5425, within the Hematology review panel as a Class II device.