FDA 510(k) Application Details - K242223

Device Classification Name	System, Imaging, Pulsed Doppler, Ultrasonic   More FDA Info for this Device
510(K) Number	K242223
Device Name	System, Imaging, Pulsed Doppler, Ultrasonic
Applicant	Supersonic Imagine 135 rue emilien gautier Aix en provence 13290 FR Other 510(k) Applications for this Company
Contact	Charlotte Turc 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	07/29/2024
Decision Date	09/20/2024
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