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Sun-Rain System Corp.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
3
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K090542SUN-RAIN ULTRASONIC THERAPY MODELS, SU-300, SU-400, SU-500, SU-600, SU-700, SU-800, SU-900October 23, 2009
K024013SUN-RAIN ULTRASONIC THERAPY, SU-100October 31, 2003
K011913SUN-TENS PALM TYPE R5/COMPACT WIRELES M2 EMS SERIESOctober 26, 2001