meddevicedb.com FDA Device Reference

PULSE ELECTRIC TOOTHBRUSH

K933829 Class I Traditional
Decision Date
1993-12-13
Sponsor / Applicant
Dentatech Corp.

Technical Specification

510(k) Submission ID K933829
Product Code JEQ
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.6865
Decision Date 1993-12-13
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

PULSE ELECTRIC TOOTHBRUSH received FDA 510(k) clearance under submission number K933829, sponsored by Dentatech 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 1993-12-13.

Classification & Regulation

This clearance is catalogued under FDA product code JEQ and 21 CFR 872.6865, within the Dental review panel as a Class I device.