Clearance Summary
PROTIME MICROCOAGULATION SYSTEM / PROTIME 3 CUVETTE received FDA 510(k) clearance under submission number K010599, sponsored by International Technidyne Corp.. The device was reviewed via the Special premarket notification pathway and assigned to the Hematology review panel. The statutory decision date of record is 2001-07-02.
- Submission: K010599
- Applicant / Sponsor: International Technidyne Corp.
- Clearance pathway: Special
- Review panel: Hematology
- Device class: Class II
- Regulation citation: 21 CFR 864.7750
- Decision date: 2001-07-02
Classification & Regulation
This clearance is catalogued under FDA product code GJS and 21 CFR 864.7750, within the Hematology review panel as a Class II device.