Clearance Summary
Type I, Type II, Type III, Type IV received FDA 510(k) clearance under submission number K172331, sponsored by Lepu Medical Technology (Beijing) 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 2018-03-02.
- Submission: K172331
- Applicant / Sponsor: Lepu Medical Technology (Beijing) Co., Ltd.
- Clearance pathway: Traditional
- Review panel: Cardiovascular
- Device class: Class II
- Regulation citation: 21 CFR 870.1340
- Decision date: 2018-03-02
Classification & Regulation
This clearance is catalogued under FDA product code DYB and 21 CFR 870.1340, within the Cardiovascular review panel as a Class II device.