FDA 510(k) Application Details - K071311

Device Classification Name	Coil, Magnetic Resonance, Specialty   More FDA Info for this Device
510(K) Number	K071311
Device Name	Coil, Magnetic Resonance, Specialty
Applicant	NEOCOIL N27 W23910A PAUL RD. PEWAUKEE, WI 53072 US Other 510(k) Applications for this Company
Contact	BRIAN BROWN 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	05/09/2007
Decision Date	05/22/2007
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