meddevicedb.com FDA Device Reference

STATUSBLUE

K013237 Class II Abbreviated
Decision Date
2001-10-22
Sponsor / Applicant
Dmg USA, Inc.

Technical Specification

510(k) Submission ID K013237
Product Code ELW
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.3660
Decision Date 2001-10-22
Clearance Pathway Abbreviated

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

STATUSBLUE received FDA 510(k) clearance under submission number K013237, sponsored by Dmg USA, Inc.. The device was reviewed via the Abbreviated premarket notification pathway and assigned to the Dental review panel. The statutory decision date of record is 2001-10-22.

Classification & Regulation

This clearance is catalogued under FDA product code ELW and 21 CFR 872.3660, within the Dental review panel as a Class II device.