Clearance Summary
AirKEE T900 received FDA 510(k) clearance under submission number K232642, sponsored by Healkee Medical Pte, Ltd.. The device was reviewed via the Traditional premarket notification pathway and assigned to the General Hospital review panel. The statutory decision date of record is 2024-05-23.
- Submission: K232642
- Applicant / Sponsor: Healkee Medical Pte, Ltd.
- Clearance pathway: Traditional
- Review panel: General Hospital
- Device class: Class II
- Regulation citation: 21 CFR 880.6500
- Decision date: 2024-05-23
Classification & Regulation
This clearance is catalogued under FDA product code FRA and 21 CFR 880.6500, within the General Hospital review panel as a Class II device.