FDA 510(k) Application Details - K222274

Device Classification Name	Unit, X-Ray, Extraoral With Timer   More FDA Info for this Device
510(K) Number	K222274
Device Name	Unit, X-Ray, Extraoral With Timer
Applicant	FONA S.r.l Via G.Galilei 11 Assago 20057 IT Other 510(k) Applications for this Company
Contact	Luigi Germano Other 510(k) Applications for this Contact
Regulation Number	872.1800   More FDA Info for this Regulation Number
Classification Product Code	EHD Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	07/29/2022
Decision Date	08/23/2022
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	DE - Dental
Review Advisory Committee	RA - Radiology
Statement / Summary / Purged Status	Summary
Type	Special
Reviewed By Third Party	N
Expedited Review