FDA 510(k) Application Details - K973842

Device Classification Name	Table, Radiographic, Stationary Top   More FDA Info for this Device
510(K) Number	K973842
Device Name	Table, Radiographic, Stationary Top
Applicant	MEDTEC, INC. 1401 8TH ST. S.E. P.O. BOX 602 ORANGE CITY, IA 51041 US Other 510(k) Applications for this Company
Contact	DONALD F RIIBE Other 510(k) Applications for this Contact
Regulation Number	892.1980   More FDA Info for this Regulation Number
Classification Product Code	IXQ Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	10/08/1997
Decision Date	12/05/1997
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