FDA 510(k) Application Details - K972451

Device Classification Name	Accelerator, Linear, Medical   More FDA Info for this Device
510(K) Number	K972451
Device Name	Accelerator, Linear, Medical
Applicant	NOMOS CORP. 2591 WEXFORD BAYNE RD. SUITE 400 SEWICKLEY, PA 15143 US Other 510(k) Applications for this Company
Contact	MARVIN L SUSSMAN 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	06/30/1997
Decision Date	01/22/1998
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