FDA 510(k) Application Details - K223470

Device Classification Name	Laser,Fluorescence Caries Detection   More FDA Info for this Device
510(K) Number	K223470
Device Name	Laser,Fluorescence Caries Detection
Applicant	SOPRO Zac Athelia IV Avenue Des Genevriers La Ciotat 13705 FR Other 510(k) Applications for this Company
Contact	Kim Rouahi Other 510(k) Applications for this Contact
Regulation Number	872.1745   More FDA Info for this Regulation Number
Classification Product Code	NBL Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	11/17/2022
Decision Date	12/14/2023
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	DE - Dental
Review Advisory Committee	DE - Dental
Statement / Summary / Purged Status	Summary
Type	Traditional
Reviewed By Third Party	N
Expedited Review