FDA 510(k) Application Details - DEN100023

Device Classification Name	More FDA Info for this Device
510(K) Number	DEN100023
Device Name	AHIP INTERNAL TRIGGER POINT WAND MODEL: 1
Applicant	NATIONAL CENTER FOR PELVIC PAIN RESEARCH DEVICES, 12470 FIORI LANE SEBASTOPOL, CA 95472 US Other 510(k) Applications for this Company
Contact	DAVID WISE Other 510(k) Applications for this Contact
Regulation Number	More FDA Info for this Regulation Number
Classification Product Code	OSD Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	08/20/2010
Decision Date	11/20/2012
Decision	DENG -
Classification Advisory Committee	PM - Physical Medicine
Review Advisory Committee	PM - Physical Medicine
Statement / Summary / Purged Status
Type	Post-NSE
Reviewed By Third Party	N
Expedited Review