meddevicedb.com FDA Device Reference

SUPERGUARD SAFETY SYRINGE

K990831 Class II Traditional
Decision Date
2000-03-08
Sponsor / Applicant
U.S. Safety Syringes Co., Inc.

Technical Specification

510(k) Submission ID K990831
Product Code MEG
Medical Specialty / Panel General Hospital
Regulation Citation 21 CFR 880.5860
Decision Date 2000-03-08
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

SUPERGUARD SAFETY SYRINGE received FDA 510(k) clearance under submission number K990831, sponsored by U.S. Safety Syringes Co., Inc.. 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 2000-03-08.

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.