FDA 510(k) Application Details - K190601

Device Classification Name	System, X-Ray, Stationary   More FDA Info for this Device
510(K) Number	K190601
Device Name	System, X-Ray, Stationary
Applicant	MedicaTech USA 50 Maxwell Irvine, CA 92618 US Other 510(k) Applications for this Company
Contact	George Makar Other 510(k) Applications for this Contact
Regulation Number	892.1680   More FDA Info for this Regulation Number
Classification Product Code	KPR Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	03/08/2019
Decision Date	04/25/2019
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