FDA 510(k) Application Details - K020400

Device Classification Name	More FDA Info for this Device
510(K) Number	K020400
Device Name	DIGITIMER D185 MULTIPULSE CORTICAL STIMULATOR
Applicant	MEPS, LLC. ONE EAST BROWARD BLVD #700 FORT LAUDERDALE, FL 33301 Other 510(k) Applications for this Company   More Company Info and Competitors
Contact	HARRY BENEDICT Other 510(k) Applications for this Contact
Regulation Number	More FDA Info for this Regulation Number
Classification Product Code	GWF Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	02/06/2002
Decision Date	08/23/2002
Decision	SE - Substantially Equivalent
Classification Advisory Committee	NE - Neurology
Review Advisory Committee	NE - Neurology
Statement / Summary / Purged Status	Statement
Type	Traditional
Reviewed By Third Party	N
Expedited Review	N