FDA 510(k) Application Details - K160350

Device Classification Name	System, X-Ray, Tomography, Computed   More FDA Info for this Device
510(K) Number	K160350
Device Name	System, X-Ray, Tomography, Computed
Applicant	NEOCOIL, LLC N27 W23910A PAUL RD. PEWAUKEE, WI 53072 US Other 510(k) Applications for this Company
Contact	MICHAEL LEIGH Other 510(k) Applications for this Contact
Regulation Number	892.1750   More FDA Info for this Regulation Number
Classification Product Code	JAK Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	02/08/2016
Decision Date	06/16/2016
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