FDA 510(k) Application Details - DEN170073

Device Classification Name	More FDA Info for this Device
510(K) Number	DEN170073
Device Name	ContaCT
Applicant	Viz.Al, Inc. 343 Texas St. San Francisco, CA 94301 US Other 510(k) Applications for this Company
Contact	Gregory Ramina Other 510(k) Applications for this Contact
Regulation Number	More FDA Info for this Regulation Number
Classification Product Code	QAS Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	09/29/2017
Decision Date	02/13/2018
Decision	DENG -
Classification Advisory Committee	RA - Radiology
Review Advisory Committee	RA - Radiology
Statement / Summary / Purged Status
Type	Direct
Reviewed By Third Party	N
Expedited Review