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MB SYSTEM, BIOENERGY LIGHT THERAPY

K030275 Class II Traditional
Decision Date
2004-11-29
Sponsor / Applicant
Amest Corp.

Technical Specification

510(k) Submission ID K030275
Product Code ILY
Medical Specialty / Panel Physical Medicine
Regulation Citation 21 CFR 890.5500
Decision Date 2004-11-29
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

MB SYSTEM, BIOENERGY LIGHT THERAPY received FDA 510(k) clearance under submission number K030275, sponsored by Amest Corp.. 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 2004-11-29.

Classification & Regulation

This clearance is catalogued under FDA product code ILY and 21 CFR 890.5500, within the Physical Medicine review panel as a Class II device.