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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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