meddevicedb.com FDA Device Reference

YIXIN SAFETY SYRINGE

K042102 Class II Traditional
Decision Date
2005-03-08
Sponsor / Applicant
Jiangxi Sanxin (Eversincere) Medical Devices Group

Technical Specification

510(k) Submission ID K042102
Product Code MEG
Medical Specialty / Panel General Hospital
Regulation Citation 21 CFR 880.5860
Decision Date 2005-03-08
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

YIXIN SAFETY SYRINGE received FDA 510(k) clearance under submission number K042102, sponsored by Jiangxi Sanxin (Eversincere) Medical Devices Group. The device was reviewed via the Traditional premarket notification pathway and assigned to the General Hospital review panel. The statutory decision date of record is 2005-03-08.

Classification & Regulation

This clearance is catalogued under FDA product code MEG and 21 CFR 880.5860, within the General Hospital review panel as a Class II device.