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SECUREGUARD RETRACTABLE SAFETY SYRINGE

K012121 Class II Traditional
Decision Date
2001-10-24
Sponsor / Applicant
Safegard Medical Products, Inc.

Technical Specification

510(k) Submission ID K012121
Product Code MEG
Medical Specialty / Panel General Hospital
Regulation Citation 21 CFR 880.5860
Decision Date 2001-10-24
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

SECUREGUARD RETRACTABLE SAFETY SYRINGE received FDA 510(k) clearance under submission number K012121, sponsored by Safegard Medical Products, 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 2001-10-24.

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.