FDA 510(k) Application Details - K192969

Device Classification Name	More FDA Info for this Device
510(K) Number	K192969
Device Name	Ezra Plexo Software
Applicant	Ezra AI Inc. 79 Madison Ave., Ste 545 New York, NY 10016 US Other 510(k) Applications for this Company
Contact	David Girard Other 510(k) Applications for this Contact
Regulation Number	More FDA Info for this Regulation Number
Classification Product Code	QIH Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	10/23/2019
Decision Date	07/10/2020
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