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MUSCLE STIMULATOR, ELECTRONIC

K781139 Class II Traditional
Decision Date
1978-09-26
Sponsor / Applicant
Thor Medical Instruments, Inc.

Technical Specification

510(k) Submission ID K781139
Product Code IPF
Medical Specialty / Panel Physical Medicine
Regulation Citation 21 CFR 890.5850
Decision Date 1978-09-26
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

MUSCLE STIMULATOR, ELECTRONIC received FDA 510(k) clearance under submission number K781139, sponsored by Thor Medical Instruments, 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 1978-09-26.

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.