FDA 510(k) Application Details - K201575

Device Classification Name	System, X-Ray, Mobile   More FDA Info for this Device
510(K) Number	K201575
Device Name	System, X-Ray, Mobile
Applicant	MinXray, Inc 3611 Commercial Ave Northbrook, IL 60062 US Other 510(k) Applications for this Company
Contact	Keith Kretchmer Other 510(k) Applications for this Contact
Regulation Number	892.1720   More FDA Info for this Regulation Number
Classification Product Code	IZL Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	06/11/2020
Decision Date	07/08/2020
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