FDA 510(k) Application Details - K112841

Device Classification Name	Accelerator, Linear, Medical   More FDA Info for this Device
510(K) Number	K112841
Device Name	Accelerator, Linear, Medical
Applicant	CALYPSO MEDICAL TECHNOLOGIES INC 2101 FOURTH AVE SUITE 500 SEATTLE, WA 98121 US Other 510(k) Applications for this Company
Contact	MARCIA PAGE Other 510(k) Applications for this Contact
Regulation Number	892.5050   More FDA Info for this Regulation Number
Classification Product Code	IYE Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	09/29/2011
Decision Date	02/16/2012
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