FDA 510(k) Application Details - K062325

Device Classification Name	Stimulator, Electrical, Transcutaneous, For Arthritis   More FDA Info for this Device
510(K) Number	K062325
Device Name	Stimulator, Electrical, Transcutaneous, For Arthritis
Applicant	RS MEDICAL P.O. BOX 3515 REDMOND, WA 98073 US Other 510(k) Applications for this Company
Contact	STEVEN CHERNOFF Other 510(k) Applications for this Contact
Regulation Number	882.5890   More FDA Info for this Regulation Number
Classification Product Code	NYN Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	08/09/2006
Decision Date	04/13/2007
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	NE - Neurology
Review Advisory Committee	NE - Neurology
Statement / Summary / Purged Status	Summary
Type	Traditional
Reviewed By Third Party	N
Expedited Review