FDA 510(k) Application Details - K233613

Device Classification Name	System, Imaging, Pulsed Echo, Ultrasonic   More FDA Info for this Device
510(K) Number	K233613
Device Name	System, Imaging, Pulsed Echo, Ultrasonic
Applicant	Siemens Medical Solutions USA, Inc. 22010 South East 51st Street Issaquah, WA 98029 US Other 510(k) Applications for this Company
Contact	Shilpa Rapaka Other 510(k) Applications for this Contact
Regulation Number	892.1560   More FDA Info for this Regulation Number
Classification Product Code	IYO Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	11/13/2023
Decision Date	06/12/2024
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	RA - Radiology
Review Advisory Committee	RA - Radiology
Statement / Summary / Purged Status	Summary
Type	Special
Reviewed By Third Party	N
Expedited Review