FDA 510(k) Application Details - K061961

Device Classification Name	System, Image Processing, Radiological   More FDA Info for this Device
510(K) Number	K061961
Device Name	System, Image Processing, Radiological
Applicant	PIE MEDICAL 11460 N. MERIDIAN ST. SUITE 150 CARMEL, IN 46032 US Other 510(k) Applications for this Company
Contact	CARRI GRAHAM 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	07/11/2006
Decision Date	09/06/2006
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