meddevicedb.com FDA Device Reference

Disposable Sterile Syringe

K221777 Class II Traditional
Decision Date
2023-10-06
Sponsor / Applicant
Weihai Shengjie Medical Technology Co., Ltd.

Technical Specification

510(k) Submission ID K221777
Product Code FMF
Medical Specialty / Panel General Hospital
Regulation Citation 21 CFR 880.5860
Decision Date 2023-10-06
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Disposable Sterile Syringe received FDA 510(k) clearance under submission number K221777, sponsored by Weihai Shengjie Medical Technology Co., Ltd.. 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 2023-10-06.

Classification & Regulation

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