meddevicedb.com FDA Device Reference

Sunmed Disposable Angio-Closure Pads

K191827 Class II Traditional
Decision Date
2020-03-16
Sponsor / Applicant
Sunny Medical Device (Shenzhen) Co., Ltd.

Technical Specification

510(k) Submission ID K191827
Product Code DXC
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.4450
Decision Date 2020-03-16
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Sunmed Disposable Angio-Closure Pads received FDA 510(k) clearance under submission number K191827, sponsored by Sunny Medical Device (Shenzhen) 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 2020-03-16.

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.