FDA 510(k) Application Details - K131685

Device Classification Name	System, Image Processing, Radiological   More FDA Info for this Device
510(K) Number	K131685
Device Name	System, Image Processing, Radiological
Applicant	GE VINGMED ULTRASOUND AS STRANDPROMENADEN 45 PO BOX 141 HORTEN N-3191 NO Other 510(k) Applications for this Company
Contact	BRYAN BEHN Other 510(k) Applications for this Contact
Regulation Number	892.2050   More FDA Info for this Regulation Number
Classification Product Code	LLZ Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	06/10/2013
Decision Date	09/24/2013
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