FDA 510(k) Application Details - K992372

Device Classification Name	Cable, Electrode   More FDA Info for this Device
510(K) Number	K992372
Device Name	Cable, Electrode
Applicant	THERAPY EQUIPMENT, INC. 13860 WELLINGTON TRACE, #310 WEST PALM BEACH, FL 33414 US Other 510(k) Applications for this Company
Contact	GLENN BUCHAN 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	07/15/1999
Decision Date	10/13/1999
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	PM - Physical Medicine
Review Advisory Committee	PM - Physical Medicine
Statement / Summary / Purged Status	Statement
Type	Traditional
Reviewed By Third Party	N
Expedited Review