FDA 510(k) Application Details - K972804

Device Classification Name	Accelerator, Linear, Medical   More FDA Info for this Device
510(K) Number	K972804
Device Name	Accelerator, Linear, Medical
Applicant	MGS RESEARCH, INC. 1 ORCHARD PARK RD., UNIT 13 MADISON, CT 06443 US Other 510(k) Applications for this Company
Contact	MAREK MARYANSKI 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	07/28/1997
Decision Date	10/23/1997
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