FDA 510(k) Application Details - K993821

Device Classification Name	Stimulator, Muscle, Powered   More FDA Info for this Device
510(K) Number	K993821
Device Name	Stimulator, Muscle, Powered
Applicant	METRON MEDICAL AUSTRALIA PTY LTD 57 ASTER AVE. CARRUM DOWNS, VICTORIA 3201 AU Other 510(k) Applications for this Company
Contact	R.H. HOPKINS 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	11/12/1999
Decision Date	12/09/1999
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