FDA 510(k) Application Details - K040122

Device Classification Name	Coil, Magnetic Resonance, Specialty   More FDA Info for this Device
510(K) Number	K040122
Device Name	Coil, Magnetic Resonance, Specialty
Applicant	Mayo Clinic 200 FIRST ST. SW ROCHESTER, MN 55905 US Other 510(k) Applications for this Company
Contact	JADE SADOSTY 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	01/20/2004
Decision Date	04/14/2004
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	RA - Radiology
Review Advisory Committee	RA - Radiology
Statement / Summary / Purged Status	Summary
Type	Special
Reviewed By Third Party	N
Expedited Review