FDA 510(k) Application Details - K072909

Device Classification Name	Coil, Magnetic Resonance, Specialty   More FDA Info for this Device
510(K) Number	K072909
Device Name	Coil, Magnetic Resonance, Specialty
Applicant	SIEMENS AG, MEDICAL SOLUTIONS HENKESTRASSE 127 ERLANGEN 91052 DE Other 510(k) Applications for this Company
Contact	LUTZ MAHN Other 510(k) Applications for this Contact
Regulation Number	892.1000   More FDA Info for this Regulation Number
Classification Product Code	MOS Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	10/12/2007
Decision Date	10/31/2007
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	Y
Expedited Review