meddevicedb.com FDA Device Reference

GINGI-PLAIN CORDS & BRAIDS

K812120 Class I Traditional
Decision Date
1981-09-08
Sponsor / Applicant
Belport Co., Inc.

Technical Specification

510(k) Submission ID K812120
Product Code JES
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.6390
Decision Date 1981-09-08
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

GINGI-PLAIN CORDS & BRAIDS received FDA 510(k) clearance under submission number K812120, sponsored by Belport Co., 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 1981-09-08.

Classification & Regulation

This clearance is catalogued under FDA product code JES and 21 CFR 872.6390, within the Dental review panel as a Class I device.