FDA 510(k) Application Details - K231573

Device Classification Name	Accelerator, Linear, Medical   More FDA Info for this Device
510(K) Number	K231573
Device Name	Accelerator, Linear, Medical
Applicant	DOSIsoft SA 45/47 Avenue Carnot Cachan 94230 FR Other 510(k) Applications for this Company
Contact	Marc Uszynski Other 510(k) Applications for this Contact
Regulation Number	892.5050   More FDA Info for this Regulation Number
Classification Product Code	IYE Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	05/31/2023
Decision Date	01/18/2024
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