FDA 510(k) Application Details - K971776

Device Classification Name	System, Image Processing, Radiological   More FDA Info for this Device
510(K) Number	K971776
Device Name	System, Image Processing, Radiological
Applicant	VMI TECHNOLOGIES 412-126 YORK ST. SUITE 412 OTTAWA,ONTARIO K1N 5T5 CA Other 510(k) Applications for this Company
Contact	DOUG SEABORN 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	05/13/1997
Decision Date	07/14/1997
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