Johari Digital Healthcare , Ltd.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
7
Inspections
4
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K131291TORC BODYJune 14, 2013
K112351ULTRA BEAUTYMarch 30, 2012
K102190WINSTIMMarch 17, 2011
K090052CRANIAL ELECTRICAL NERVE STIMULATOR, MODEL FM 10/CMay 29, 2009
K062439POWERTONE, MODEL PT-11January 8, 2007
K060246INFREXMay 5, 2006
K024036PRODUCT LINE-COMBO STIMULATOR/SEQUENTIAL STIMULATOR, MODEL IF-5000December 20, 2002