FDA 510(k) Application Details - K080223

Device Classification Name	System, Imaging, Pulsed Echo, Ultrasonic   More FDA Info for this Device
510(K) Number	K080223
Device Name	System, Imaging, Pulsed Echo, Ultrasonic
Applicant	IMACOR LLC 1835 MARKET STREET 28TH FLOOR PHILADELPHIA, PA 19103 US Other 510(k) Applications for this Company
Contact	STEVEN B DATLOF M.D., J.D. 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	01/29/2008
Decision Date	06/24/2008
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