FDA 510(k) Application Details - K142421

Device Classification Name	System, Nuclear Magnetic Resonance Imaging   More FDA Info for this Device
510(K) Number	K142421
Device Name	System, Nuclear Magnetic Resonance Imaging
Applicant	ESAOTE, S.P.A. VIA SIFFREDI 58 GENOVA 16153 IT Other 510(k) Applications for this Company
Contact	Donatella Ragghianti Other 510(k) Applications for this Contact
Regulation Number	892.1000   More FDA Info for this Regulation Number
Classification Product Code	LNH Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	08/28/2014
Decision Date	04/09/2015
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	N
Expedited Review