FDA 510(k) Application Details - K210921

Device Classification Name	Accelerator, Linear, Medical   More FDA Info for this Device
510(K) Number	K210921
Device Name	Accelerator, Linear, Medical
Applicant	Our United Corporation Room 10301, 3rd Floor, Unit 1, Block 28, ShouChuang International Business Center, No.66 Xi'an 710018 CN Other 510(k) Applications for this Company
Contact	Qi Liu 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	03/29/2021
Decision Date	11/02/2021
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