FDA 510(k) Application Details - K001833

Device Classification Name	Accelerator, Linear, Medical   More FDA Info for this Device
510(K) Number	K001833
Device Name	Accelerator, Linear, Medical
Applicant	NORTHWEST MEDICAL PHYSICS EQUIPMENT, INC. 21031 67TH AVE. WEST LYNNWOOD, WA 98036 US Other 510(k) Applications for this Company
Contact	LEE MYERS 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	06/16/2000
Decision Date	09/28/2000
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	RA - Radiology
Review Advisory Committee	RA - Radiology
Statement / Summary / Purged Status	Summary
Type	Special
Reviewed By Third Party	N
Expedited Review