FDA 510(k) Application Details - K030869

Device Classification Name	Device, Muscle Monitoring   More FDA Info for this Device
510(K) Number	K030869
Device Name	Device, Muscle Monitoring
Applicant	S.L.P. LTD. 18 HAZFIRA ST. TEL-AVIV 67779 IL Other 510(k) Applications for this Company
Contact	TAMAR SHOCHAT Other 510(k) Applications for this Contact
Regulation Number	890.1375   More FDA Info for this Regulation Number
Classification Product Code	KZM Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	03/19/2003
Decision Date	05/14/2004
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	PM - Physical Medicine
Review Advisory Committee	DE - Dental
Statement / Summary / Purged Status	Summary
Type	Traditional
Reviewed By Third Party	N
Expedited Review