FDA 510(k) Application Details - K150239

Device Classification Name	System, Imaging, Pulsed Echo, Ultrasonic   More FDA Info for this Device
510(K) Number	K150239
Device Name	System, Imaging, Pulsed Echo, Ultrasonic
Applicant	Echosens 30 Place d'Italia Paris 75013 FR Other 510(k) Applications for this Company
Contact	Celine Fournier 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	02/02/2015
Decision Date	09/01/2015
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