FDA 510(k) Application Details - K964025

Device Classification Name	Grid, Radiographic   More FDA Info for this Device
510(K) Number	K964025
Device Name	Grid, Radiographic
Applicant	X-RAY ACCESSORY CORP. 207 DAY ST. DANIELSON, CT 06239-2313 US Other 510(k) Applications for this Company
Contact	WILLIAM HAGUE Other 510(k) Applications for this Contact
Regulation Number	892.1910   More FDA Info for this Regulation Number
Classification Product Code	IXJ Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	10/07/1996
Decision Date	06/13/1997
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