meddevicedb.com FDA Device Reference

Sunmed Control Syringes

K160190 Class II Traditional
Decision Date
2016-11-10
Sponsor / Applicant
Sunny Medical Device (Shenzhen) Co., Ltd.

Technical Specification

510(k) Submission ID K160190
Product Code DXT
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.1650
Decision Date 2016-11-10
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Sunmed Control Syringes received FDA 510(k) clearance under submission number K160190, 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 2016-11-10.

Classification & Regulation

This clearance is catalogued under FDA product code DXT and 21 CFR 870.1650, within the Cardiovascular review panel as a Class II device.