FDA 510(k) Application Details - K233439

Device Classification Name	System, Imaging, Pulsed Doppler, Ultrasonic   More FDA Info for this Device
510(K) Number	K233439
Device Name	System, Imaging, Pulsed Doppler, Ultrasonic
Applicant	Qingdao Hisense Medical Equipment Co., Ltd No. 399 Songling Road, Laoshan District Qingdao 266100 CN Other 510(k) Applications for this Company
Contact	Yalan Wu Other 510(k) Applications for this Contact
Regulation Number	892.1550   More FDA Info for this Regulation Number
Classification Product Code	IYN Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	10/16/2023
Decision Date	02/21/2024
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