meddevicedb.com FDA Device Reference

HIGH VOLTAGE GALVANIC STIMULATOR 550

K813456 Class II Traditional
Decision Date
1982-01-29
Sponsor / Applicant
Chattanooga Group, Inc.

Technical Specification

510(k) Submission ID K813456
Product Code IPF
Medical Specialty / Panel Physical Medicine
Regulation Citation 21 CFR 890.5850
Decision Date 1982-01-29
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

HIGH VOLTAGE GALVANIC STIMULATOR 550 received FDA 510(k) clearance under submission number K813456, sponsored by Chattanooga Group, 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 1982-01-29.

Classification & Regulation

This clearance is catalogued under FDA product code IPF and 21 CFR 890.5850, within the Physical Medicine review panel as a Class II device.