FDA 510(k) Application Details - K052610

Device Classification Name	System, X-Ray, Fluoroscopic, Image-Intensified   More FDA Info for this Device
510(K) Number	K052610
Device Name	System, X-Ray, Fluoroscopic, Image-Intensified
Applicant	LAKESHORE TECHNOLOGIES INC. 7536 MURRAY DR. CICERO, NY 13039 US Other 510(k) Applications for this Company
Contact	JACK RACE Other 510(k) Applications for this Contact
Regulation Number	892.1650   More FDA Info for this Regulation Number
Classification Product Code	JAA Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	09/22/2005
Decision Date	11/30/2005
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