Clearance Summary
The IQool System received FDA 510(k) clearance under submission number K162523, sponsored by Braincool AB. The device was reviewed via the Traditional premarket notification pathway and assigned to the Cardiovascular review panel. The statutory decision date of record is 2017-05-03.
- Submission: K162523
- Applicant / Sponsor: Braincool AB
- Clearance pathway: Traditional
- Review panel: Cardiovascular
- Device class: Class II
- Regulation citation: 21 CFR 870.5900
- Decision date: 2017-05-03
Classification & Regulation
This clearance is catalogued under FDA product code NZE and 21 CFR 870.5900, within the Cardiovascular review panel as a Class II device.