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ELECTRONIC CELL ENERGIZER

K834293 Class II Traditional
Decision Date
1984-01-13
Sponsor / Applicant
Electronic Energy, Inc.

Technical Specification

510(k) Submission ID K834293
Product Code LBG
Medical Specialty / Panel Physical Medicine
Regulation Citation 21 CFR 890.5500
Decision Date 1984-01-13
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

ELECTRONIC CELL ENERGIZER received FDA 510(k) clearance under submission number K834293, sponsored by Electronic Energy, 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 1984-01-13.

Classification & Regulation

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