FDA 510(k) Application Details - K062532

Device Classification Name	Stimulator, Nerve, Transcutaneous, Over-The-Counter   More FDA Info for this Device
510(K) Number	K062532
Device Name	Stimulator, Nerve, Transcutaneous, Over-The-Counter
Applicant	PAIN RELIEF TECHNOLOGIES 15048 SW CAPSTONE CT. BEAVERTON, OR 97007 US Other 510(k) Applications for this Company
Contact	KENDALL GORHAM Other 510(k) Applications for this Contact
Regulation Number	882.5890   More FDA Info for this Regulation Number
Classification Product Code	NUH Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	08/28/2006
Decision Date	02/09/2007
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	NE - Neurology
Review Advisory Committee	NE - Neurology
Statement / Summary / Purged Status	Statement
Type	Traditional
Reviewed By Third Party	N
Expedited Review