FDA 510(k) Application Details - K961193

Device Classification Name	System, X-Ray, Fluoroscopic, Image-Intensified   More FDA Info for this Device
510(K) Number	K961193
Device Name	System, X-Ray, Fluoroscopic, Image-Intensified
Applicant	XRE CORP. 300 FOSTER ST. LITTLETON, MA 01460-2017 US Other 510(k) Applications for this Company
Contact	WAYNE V LOOMER 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	03/21/1996
Decision Date	06/17/1996
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	RA - Radiology
Review Advisory Committee	RA - Radiology
Statement / Summary / Purged Status	Statement
Type	Traditional
Reviewed By Third Party	N
Expedited Review