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SONICWAVE SONIC PLAQUE REMOVER

K012914 Class I Traditional
Decision Date
2001-10-01
Sponsor / Applicant
Homedics, Inc.

Technical Specification

510(k) Submission ID K012914
Product Code JEQ
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.6865
Decision Date 2001-10-01
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

SONICWAVE SONIC PLAQUE REMOVER received FDA 510(k) clearance under submission number K012914, sponsored by Homedics, 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 2001-10-01.

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.