meddevicedb.com FDA Device Reference

MIRAMATIC SAFE SYRINGE SYSTEM

K043322 Class II Traditional
Decision Date
2005-07-21
Sponsor / Applicant
Hager Worldwide, Inc.

Technical Specification

510(k) Submission ID K043322
Product Code EJI
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.6770
Decision Date 2005-07-21
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

MIRAMATIC SAFE SYRINGE SYSTEM received FDA 510(k) clearance under submission number K043322, sponsored by Hager Worldwide, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Dental review panel. The statutory decision date of record is 2005-07-21.

Classification & Regulation

This clearance is catalogued under FDA product code EJI and 21 CFR 872.6770, within the Dental review panel as a Class II device.