meddevicedb.com FDA Device Reference

RUBBER DAM

K780745 Class I Traditional
Decision Date
1978-05-12
Sponsor / Applicant
Hygienic Dental Mfg., Co., The

Technical Specification

510(k) Submission ID K780745
Product Code EIE
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.6300
Decision Date 1978-05-12
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

RUBBER DAM received FDA 510(k) clearance under submission number K780745, sponsored by Hygienic Dental Mfg., Co., The. The device was reviewed via the Traditional premarket notification pathway and assigned to the Dental review panel. The statutory decision date of record is 1978-05-12.

Classification & Regulation

This clearance is catalogued under FDA product code EIE and 21 CFR 872.6300, within the Dental review panel as a Class I device.