meddevicedb.com FDA Device Reference

ELECTRIC MUSCLE STIMULATOR

K813533 Class II Traditional
Decision Date
1982-03-05
Sponsor / Applicant
Myo-Tronics Research, Inc.

Technical Specification

510(k) Submission ID K813533
Product Code IPF
Medical Specialty / Panel Physical Medicine
Regulation Citation 21 CFR 890.5850
Decision Date 1982-03-05
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

ELECTRIC MUSCLE STIMULATOR received FDA 510(k) clearance under submission number K813533, sponsored by Myo-Tronics Research, 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 1982-03-05.

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.