FDA 510(k) Application Details - K973223

Device Classification Name	Stimulator, Muscle, Powered   More FDA Info for this Device
510(K) Number	K973223
Device Name	Stimulator, Muscle, Powered
Applicant	STELLAR MEDICAL CORP. 12300 TWINBROOK PKWY, STE. 625 ROCKVILLE, MD 20852 US Other 510(k) Applications for this Company
Contact	T. WHIT ATHEY 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	08/27/1997
Decision Date	02/18/1998
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