FDA 510(k) Application Details - K240808

Device Classification Name	Oximeter   More FDA Info for this Device
510(K) Number	K240808
Device Name	Oximeter
Applicant	Hunan Accurate Bio-Medical Technology Co., Ltd. Accurate Industrial Park, No.108, Zhixian Rd Xuelian Community, Xueshi Street of Yuelu District, Changsha 410208 CN Other 510(k) Applications for this Company
Contact	Li Zhang 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	03/25/2024
Decision Date	10/03/2024
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