FDA 510(k) Application Details - K201019

Device Classification Name	More FDA Info for this Device
510(K) Number	K201019
Device Name	Genius AI Detection
Applicant	Hologic, Inc. 250 Campus Drive Marlborough, MA 01752 US Other 510(k) Applications for this Company
Contact	Deborah Thomas Other 510(k) Applications for this Contact
Regulation Number	More FDA Info for this Regulation Number
Classification Product Code	QDQ Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	04/17/2020
Decision Date	11/18/2020
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