FDA 510(k) Application Details - K983902

Device Classification Name	System, Nuclear Magnetic Resonance Imaging   More FDA Info for this Device
510(K) Number	K983902
Device Name	System, Nuclear Magnetic Resonance Imaging
Applicant	INTERMAGNETICS GENERAL CORP. 450 OLD NISKAYUNA RD. P.O. BOX 461 LATHAM, NY 12110-0461 US Other 510(k) Applications for this Company
Contact	IAN L PYKETT Other 510(k) Applications for this Contact
Regulation Number	892.1000   More FDA Info for this Regulation Number
Classification Product Code	LNH Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	11/03/1998
Decision Date	01/07/1999
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