FDA 510(k) Application Details - K060236

Device Classification Name	Device, Iontophoresis, Other Uses   More FDA Info for this Device
510(K) Number	K060236
Device Name	Device, Iontophoresis, Other Uses
Applicant	IOMED, INC. 2441 SOUTH 3850 WEST, SUITE A SALT LAKE CITY, UT 84120-9941 US Other 510(k) Applications for this Company
Contact	CURTIS JENSEN Other 510(k) Applications for this Contact
Regulation Number	890.5525   More FDA Info for this Regulation Number
Classification Product Code	EGJ Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	01/30/2006
Decision Date	03/31/2006
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	PM - Physical Medicine
Review Advisory Committee	PM - Physical Medicine
Statement / Summary / Purged Status	Summary
Type	Traditional
Reviewed By Third Party	N
Expedited Review