THERMASSAGE ENERGY PRODUCT, MODEL HY5000— 510(k) K032449

Name: FDA 510(k) clearance K032449
Creator: U.S. Food and Drug Administration
Published: 2003-10-22

Substantially Equivalent

Migun Medical Instrument Co. , Ltd.

FDA 510(k) clearance K032449 for THERMASSAGE ENERGY PRODUCT, MODEL HY5000, Substantially Equivalent on 2003-10-22. Applicant: Migun Medical Instrument Co. , Ltd.. Device class: 2.

Clearance details

Applicant: Migun Medical Instrument Co. , Ltd.
Product code: Code JFB
Device class: Class 2
Regulation: 21 CFR 890.5880
Advisory panel: Physical Medicine
Date received: 2003-08-08
Decision date: 2003-10-22
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Cleveland, OH, US

Download summary PDF View on FDA.gov ↗

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