FDA 510(k) Application Details - K230144

Device Classification Name	Analyzer,Medical Image   More FDA Info for this Device
510(K) Number	K230144
Device Name	Analyzer,Medical Image
Applicant	Denti.AI Technology, Inc. 99 Yorkville Ave, Suite 214 Toronto M5R3k5 CA Other 510(k) Applications for this Company
Contact	Lyudmila Tuzova Other 510(k) Applications for this Contact
Regulation Number	000.0000   More FDA Info for this Regulation Number
Classification Product Code	MYN Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	01/18/2023
Decision Date	10/06/2023
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