FDA 510(k) Application Details - K083502

Device Classification Name	System,Planning,Radiation Therapy Treatment   More FDA Info for this Device
510(K) Number	K083502
Device Name	System,Planning,Radiation Therapy Treatment
Applicant	PROWESS, INC. 5063 COMMERCIAL CIRCLE SUITE A&B CONCORD, CA 94520 US Other 510(k) Applications for this Company
Contact	RACHEL SCARANO 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	11/25/2008
Decision Date	05/05/2009
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	RA - Radiology
Review Advisory Committee	RA - Radiology
Statement / Summary / Purged Status	Summary
Type	Traditional
Reviewed By Third Party	N
Expedited Review