Clearance Summary
HEMOSIL D-DIMER HS 500 CONTROL received FDA 510(k) clearance under submission number K133582, sponsored by Instrumentation Laboratory. The device was reviewed via the Traditional premarket notification pathway and assigned to the Hematology review panel. The statutory decision date of record is 2014-08-15.
- Submission: K133582
- Applicant / Sponsor: Instrumentation Laboratory
- Clearance pathway: Traditional
- Review panel: Hematology
- Device class: Class II
- Regulation citation: 21 CFR 864.5425
- Decision date: 2014-08-15
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.