FDA 510(k) Application Details - K080219

Device Classification Name	Stimulator, Neuromuscular, External Functional   More FDA Info for this Device
510(K) Number	K080219
Device Name	Stimulator, Neuromuscular, External Functional
Applicant	NESS-NEUROMUSCULAR ELECTRICAL STIMULATION SYSTEMS 25103 RYE CANYON LOOP VALENCIA, CA 91355 US Other 510(k) Applications for this Company
Contact	EVAN ROSENFELD Other 510(k) Applications for this Contact
Regulation Number	882.5810   More FDA Info for this Regulation Number
Classification Product Code	GZI Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	01/29/2008
Decision Date	02/28/2008
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	NE - Neurology
Review Advisory Committee	NE - Neurology
Statement / Summary / Purged Status	Summary
Type	Special
Reviewed By Third Party	N
Expedited Review