meddevicedb.com FDA Device Reference

CYNOSURE TRIACTIVE THERAPEUTIC MASSAGE SYSTEM

K030876 Class I Traditional
Decision Date
2004-01-22
Sponsor / Applicant
Cynosure, Inc.

Technical Specification

510(k) Submission ID K030876
Product Code ISA
Medical Specialty / Panel Physical Medicine
Regulation Citation 21 CFR 890.5660
Decision Date 2004-01-22
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

CYNOSURE TRIACTIVE THERAPEUTIC MASSAGE SYSTEM received FDA 510(k) clearance under submission number K030876, sponsored by Cynosure, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Physical Medicine review panel. The statutory decision date of record is 2004-01-22.

Classification & Regulation

This clearance is catalogued under FDA product code ISA and 21 CFR 890.5660, within the Physical Medicine review panel as a Class I device.