FDA 510(k) Application Details - K081112

Device Classification Name	System,Planning,Radiation Therapy Treatment   More FDA Info for this Device
510(K) Number	K081112
Device Name	System,Planning,Radiation Therapy Treatment
Applicant	ISODOSE CONTROL B.V. LANDJUWEEL 11 VEENENDAAL 3905 PE NL Other 510(k) Applications for this Company
Contact	HUB VAN DE BERGH Other 510(k) Applications for this Contact
Regulation Number	892.5050   More FDA Info for this Regulation Number
Classification Product Code	MUJ Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	04/18/2008
Decision Date	07/29/2008
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	RA - Radiology
Review Advisory Committee	RA - Radiology
Statement / Summary / Purged Status	Summary
Type	Abbreviated
Reviewed By Third Party	N
Expedited Review