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Sterile Safety Syringe with Needle for Single Use, Sterile Safety Hypodermic Needle for Single Use,Sterile Auto-Disable Syringe with Needle for Single Use

K212920 Class II Traditional
Decision Date
2022-03-11
Sponsor / Applicant
Shandong Weigao Group Medical Polymer Co., Ltd.

Technical Specification

510(k) Submission ID K212920
Product Code FMF
Medical Specialty / Panel General Hospital
Regulation Citation 21 CFR 880.5860
Decision Date 2022-03-11
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Sterile Safety Syringe with Needle for Single Use, Sterile Safety Hypodermic Needle for Single Use,Sterile Auto-Disable Syringe with Needle for Single Use received FDA 510(k) clearance under submission number K212920, sponsored by Shandong Weigao Group Medical Polymer 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 2022-03-11.

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.