SUN-RAIN ULTRASONIC THERAPY MODELS, SU-300, SU-400, SU-500, SU-600, SU-700, SU-800, SU-900— 510(k) K090542

Name: FDA 510(k) clearance K090542
Creator: U.S. Food and Drug Administration
Published: 2009-10-23

Substantially Equivalent

Sun-Rain System Corp.

FDA 510(k) clearance K090542 for SUN-RAIN ULTRASONIC THERAPY MODELS, SU-300, SU-400, SU-500, SU-600, SU-700, SU-800, SU-900, Substantially Equivalent on 2009-10-23. Applicant: Sun-Rain System Corp.. Device class: 2.

Clearance details

Applicant: Sun-Rain System Corp.
Product code: Code IMI
Device class: Class 2
Regulation: 21 CFR 890.5300
Advisory panel: Physical Medicine
Date received: 2009-03-02
Decision date: 2009-10-23
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Hsin-Chu City, TW

Download summary PDF View on FDA.gov ↗

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Data sourced from openFDA. This site is unofficial and independent of the FDA.