FDA 510(k) Application Details - K993742

Device Classification Name	Accelerator, Linear, Medical   More FDA Info for this Device
510(K) Number	K993742
Device Name	Accelerator, Linear, Medical
Applicant	I.Z.I. CORP. P.O. BOX 4321 CROFTON, MD 21114 US Other 510(k) Applications for this Company
Contact	E.J. Smith 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	11/04/1999
Decision Date	02/02/2000
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	RA - Radiology
Review Advisory Committee	RA - Radiology
Statement / Summary / Purged Status	Statement
Type	Traditional
Reviewed By Third Party	N
Expedited Review