FDA 510(k) Application Details - K984023

Device Classification Name	System, Image Processing, Radiological   More FDA Info for this Device
510(K) Number	K984023
Device Name	System, Image Processing, Radiological
Applicant	DYNAMIC HEALTHCARE TECHNOLOGIES, INC. 615 CRESCENT EXECUTIVE CT. 5TH FLR. LAKE MARY, FL 32746-2109 US Other 510(k) Applications for this Company
Contact	KAREN W WHITE 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	11/12/1998
Decision Date	12/08/1998
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	RA - Radiology
Review Advisory Committee	RA - Radiology
Statement / Summary / Purged Status	Summary
Type	Special
Reviewed By Third Party	N
Expedited Review