meddevicedb.com FDA Device Reference

BEACH CURETTE NO. 2 AND NO. 3 T.G.

K821789 Class I Traditional
Decision Date
1982-07-06
Sponsor / Applicant
Pacific Dental Corp.

Technical Specification

510(k) Submission ID K821789
Product Code EMS
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.4565
Decision Date 1982-07-06
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

BEACH CURETTE NO. 2 AND NO. 3 T.G. received FDA 510(k) clearance under submission number K821789, sponsored by Pacific Dental Corp.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Dental review panel. The statutory decision date of record is 1982-07-06.

Classification & Regulation

This clearance is catalogued under FDA product code EMS and 21 CFR 872.4565, within the Dental review panel as a Class I device.