FDA 510(k) Application Details - K070926

Device Classification Name	Cable, Electrode   More FDA Info for this Device
510(K) Number	K070926
Device Name	Cable, Electrode
Applicant	Oscor Inc. 3816 DE SOTO BLVD. PALM HARBOR, FL 34683 US Other 510(k) Applications for this Company
Contact	MILA DOSKOCIL Other 510(k) Applications for this Contact
Regulation Number	890.1175   More FDA Info for this Regulation Number
Classification Product Code	IKD Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	04/03/2007
Decision Date	06/07/2007
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	PM - Physical Medicine
Review Advisory Committee	PM - Physical Medicine
Statement / Summary / Purged Status	Statement
Type	Special
Reviewed By Third Party	N
Expedited Review