DYNASOUND MODEL 401 THERAPEUTIC ULTRASOUND STIMULATOR— 510(k) K934287

Name: FDA 510(k) clearance K934287
Creator: U.S. Food and Drug Administration
Published: 1994-04-04

Substantially Equivalent

Dynawave, Corp.

FDA 510(k) clearance K934287 for DYNASOUND MODEL 401 THERAPEUTIC ULTRASOUND STIMULATOR, Substantially Equivalent on 1994-04-04. Applicant: Dynawave, Corp.. Device class: 2.

Clearance details

Applicant: Dynawave, Corp.
Product code: Code IMG
Device class: Class 2
Regulation: 21 CFR 890.5860
Advisory panel: Physical Medicine
Date received: 1993-09-02
Decision date: 1994-04-04
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Geneva, IL, US

Download summary PDF View on FDA.gov ↗

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