FDA 510(k) Application Details - K232975

Device Classification Name	Oximeter   More FDA Info for this Device
510(K) Number	K232975
Device Name	Oximeter
Applicant	Beijing Choice Electronic Technology Co., Ltd. 2nd Floor, 3rd Floor and Room 410-412 4th Floor No. 2 Building, No. 9 Shuangyuan Road Beijing 100041 CN Other 510(k) Applications for this Company
Contact	Haiying Zhao Other 510(k) Applications for this Contact
Regulation Number	870.2700   More FDA Info for this Regulation Number
Classification Product Code	DQA Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	09/21/2023
Decision Date	06/21/2024
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	CV - Cardiovascular
Review Advisory Committee	AN - Anesthesiology
Statement / Summary / Purged Status	Summary
Type	Traditional
Reviewed By Third Party	N
Expedited Review