FDA 510(k) Application Details - K024352

Device Classification Name	Coil, Magnetic Resonance, Specialty   More FDA Info for this Device
510(K) Number	K024352
Device Name	Coil, Magnetic Resonance, Specialty
Applicant	MRI DEVICES CORP. 1515 PARAMOUNT DR. WAUKESHA, WI 53186 US Other 510(k) Applications for this Company
Contact	THOMAS SCHUBERT 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	12/30/2002
Decision Date	01/09/2003
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	RA - Radiology
Review Advisory Committee	RA - Radiology
Statement / Summary / Purged Status	Statement
Type	Special
Reviewed By Third Party	N
Expedited Review