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DYNASOUND MODEL 401 THERAPEUTIC ULTRASOUND STIMULATOR

K934287 Class II Traditional
Decision Date
1994-04-04
Sponsor / Applicant
Dynawave, Corp.

Technical Specification

510(k) Submission ID K934287
Product Code IMG
Medical Specialty / Panel Physical Medicine
Regulation Citation 21 CFR 890.5860
Decision Date 1994-04-04
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

DYNASOUND MODEL 401 THERAPEUTIC ULTRASOUND STIMULATOR received FDA 510(k) clearance under submission number K934287, sponsored by Dynawave, Corp.. 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 1994-04-04.

Classification & Regulation

This clearance is catalogued under FDA product code IMG and 21 CFR 890.5860, within the Physical Medicine review panel as a Class II device.