Clearance Summary
IntelliCuff received FDA 510(k) clearance under submission number K150893, sponsored by Hamilton Medical AG. The device was reviewed via the Traditional premarket notification pathway and assigned to the Anesthesiology review panel. The statutory decision date of record is 2016-01-29.
- Submission: K150893
- Applicant / Sponsor: Hamilton Medical AG
- Clearance pathway: Traditional
- Review panel: Anesthesiology
- Device class: Class II
- Regulation citation: 21 CFR 868.5750
- Decision date: 2016-01-29
Classification & Regulation
This clearance is catalogued under FDA product code BSK and 21 CFR 868.5750, within the Anesthesiology review panel as a Class II device.