FDA 510(k) Application Details - K091645

Device Classification Name	Accelerator, Linear, Medical   More FDA Info for this Device
510(K) Number	K091645
Device Name	Accelerator, Linear, Medical
Applicant	NASLUND MEDICAL AB VASSVAGEN 21 HUDDINGE 14139 SE Other 510(k) Applications for this Company
Contact	TOMAS NASLUND 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	06/04/2009
Decision Date	07/21/2009
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