FDA 510(k) Application Details - K010888

Device Classification Name	Set, Administration, Intravascular   More FDA Info for this Device
510(K) Number	K010888
Device Name	Set, Administration, Intravascular
Applicant	MEDIVICE SYSTEMS, LTD. BEIT HAPA'AMON (BOX 124) 20 HATA'AS ST. KFAR SABA 44425 IL Other 510(k) Applications for this Company
Contact	AHAVA STEIN Other 510(k) Applications for this Contact
Regulation Number	880.5440   More FDA Info for this Regulation Number
Classification Product Code	FPA Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	03/23/2001
Decision Date	06/27/2001
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	HO - General Hospital
Review Advisory Committee	HO - General Hospital
Statement / Summary / Purged Status	Statement
Type	Traditional
Reviewed By Third Party	N
Expedited Review