FDA 510(k) Application Details - K041953

Device Classification Name	Electrode, Cutaneous   More FDA Info for this Device
510(K) Number	K041953
Device Name	Electrode, Cutaneous
Applicant	CONMED CORP. 525 FRENCH RD. UTICA, NY 13502 US Other 510(k) Applications for this Company
Contact	IRA DUESLER Other 510(k) Applications for this Contact
Regulation Number	882.1320   More FDA Info for this Regulation Number
Classification Product Code	GXY Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	07/20/2004
Decision Date	08/09/2004
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	NE - Neurology
Review Advisory Committee	NE - Neurology
Statement / Summary / Purged Status	Statement
Type	Special
Reviewed By Third Party	N
Expedited Review