meddevicedb.com FDA Device Reference

RE NU

K973289 Class I Traditional
Decision Date
1999-02-09
Sponsor / Applicant
Pacific Rim Dental, Inc.

Technical Specification

510(k) Submission ID K973289
Product Code EJR
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.6030
Decision Date 1999-02-09
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

RE NU received FDA 510(k) clearance under submission number K973289, sponsored by Pacific Rim Dental, 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 1999-02-09.

Classification & Regulation

This clearance is catalogued under FDA product code EJR and 21 CFR 872.6030, within the Dental review panel as a Class I device.