Clearance Summary
Med-link Reusable Blood Pressure Cuff received FDA 510(k) clearance under submission number K173869, sponsored by Shenzhen Med-Link Electronics Tech Co., Ltd.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Cardiovascular review panel. The statutory decision date of record is 2018-08-02.
- Submission: K173869
- Applicant / Sponsor: Shenzhen Med-Link Electronics Tech Co., Ltd.
- Clearance pathway: Traditional
- Review panel: Cardiovascular
- Device class: Class II
- Regulation citation: 21 CFR 870.1120
- Decision date: 2018-08-02
Classification & Regulation
This clearance is catalogued under FDA product code DXQ and 21 CFR 870.1120, within the Cardiovascular review panel as a Class II device.