Clearance Summary
HEMOCHRON(R) HEPARIN RESPONSE TEST received FDA 510(k) clearance under submission number K904003, sponsored by Intensive Technology, 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 1990-11-29.
- Submission: K904003
- Applicant / Sponsor: Intensive Technology, Inc.
- Clearance pathway: Traditional
- Review panel: Hematology
- Device class: Class II
- Regulation citation: 21 CFR 864.7525
- Decision date: 1990-11-29
Classification & Regulation
This clearance is catalogued under FDA product code KFF and 21 CFR 864.7525, within the Hematology review panel as a Class II device.