FDA 510(k) Applications Submitted by SUN-RAIN SYSTEM CORP.

FDA 510(k) Number Submission Date Device Name Applicant
K090542 03/02/2009 SUN-RAIN ULTRASONIC THERAPY MODELS, SU-300, SU-400, SU-500, SU-600, SU-700, SU-800, SU-900 SUN-RAIN SYSTEM CORP.
K024013 12/04/2002 SUN-RAIN ULTRASONIC THERAPY, SU-100 SUN-RAIN SYSTEM CORP.
K011913 06/19/2001 SUN-TENS PALM TYPE R5/COMPACT WIRELES M2 EMS SERIES SUN-RAIN SYSTEM CORP.


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