FDA 510(k) Application Details - K222666

Device Classification Name	X-Ray, Tomography, Computed, Dental   More FDA Info for this Device
510(K) Number	K222666
Device Name	X-Ray, Tomography, Computed, Dental
Applicant	Trident s.r.l Via Artigiani 4 Castenedolo 25014 IT Other 510(k) Applications for this Company
Contact	Giorgio Rizzo Other 510(k) Applications for this Contact
Regulation Number	892.1750   More FDA Info for this Regulation Number
Classification Product Code	OAS Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	09/06/2022
Decision Date	07/10/2023
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