meddevicedb.com FDA Device Reference

Vasc Band hemostat

K142359 Class II Traditional
Decision Date
2014-10-23
Sponsor / Applicant
Lepu Medical Technology (Beijing) Co., Ltd.

Technical Specification

510(k) Submission ID K142359
Product Code DXC
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.4450
Decision Date 2014-10-23
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Vasc Band hemostat received FDA 510(k) clearance under submission number K142359, 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 2014-10-23.

Classification & Regulation

This clearance is catalogued under FDA product code DXC and 21 CFR 870.4450, within the Cardiovascular review panel as a Class II device.