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ULTRASONIC THERAPY APPARATUS, 407

K781317 Class II Traditional
Decision Date
1978-10-03
Sponsor / Applicant
General Theraphysical, Inc.

Technical Specification

510(k) Submission ID K781317
Product Code IMI
Medical Specialty / Panel Physical Medicine
Regulation Citation 21 CFR 890.5300
Decision Date 1978-10-03
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

ULTRASONIC THERAPY APPARATUS, 407 received FDA 510(k) clearance under submission number K781317, sponsored by General Theraphysical, 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 1978-10-03.

Classification & Regulation

This clearance is catalogued under FDA product code IMI and 21 CFR 890.5300, within the Physical Medicine review panel as a Class II device.