FDA 510(k) Application Details - K952273

Device Classification Name	Stimulator, Muscle, Powered   More FDA Info for this Device
510(K) Number	K952273
Device Name	Stimulator, Muscle, Powered
Applicant	NEUROMUSCLAR ELECTRICAL STIMULATION SYSTEMS, LTD. 555 THIRTEENTH STREET, N.W. WASHINGTON, DC 20004 US Other 510(k) Applications for this Company
Contact	HOWARD M HOLSTEIN Other 510(k) Applications for this Contact
Regulation Number	890.5850   More FDA Info for this Regulation Number
Classification Product Code	IPF Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	05/15/1995
Decision Date	05/23/1996
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	PM - Physical Medicine
Review Advisory Committee	PM - Physical Medicine
Statement / Summary / Purged Status	Summary
Type	Traditional
Reviewed By Third Party	N
Expedited Review