Clearance Summary
AIK Sterile Acupuncture Needles for Single Use received FDA 510(k) clearance under submission number K162566, sponsored by Changchun Aik Medical Devices Co., 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 2017-05-11.
- Submission: K162566
- Applicant / Sponsor: Changchun Aik Medical Devices Co., Ltd.
- Clearance pathway: Traditional
- Review panel: General Hospital
- Device class: Class II
- Regulation citation: 21 CFR 880.5580
- Decision date: 2017-05-11
Classification & Regulation
This clearance is catalogued under FDA product code MQX and 21 CFR 880.5580, within the General Hospital review panel as a Class II device.