FDA 510(k) Application Details - K062767

Device Classification Name	Coil, Magnetic Resonance, Specialty   More FDA Info for this Device
510(K) Number	K062767
Device Name	Coil, Magnetic Resonance, Specialty
Applicant	INVIVO CORPORATION N27 W23676 PAUL RD. PEWAUKEE, WI 53072 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	09/15/2006
Decision Date	10/13/2006
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