FDA 510(k) Application Details - K955414

Device Classification Name	Table, Radiologic   More FDA Info for this Device
510(K) Number	K955414
Device Name	Table, Radiologic
Applicant	WUESTEC MEDICAL, INC. 421 HOLCOLMBE AVE. MOBILE, AL 36606 US Other 510(k) Applications for this Company
Contact	JIM MILLER Other 510(k) Applications for this Contact
Regulation Number	892.1980   More FDA Info for this Regulation Number
Classification Product Code	KXJ Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	11/27/1995
Decision Date	07/24/1996
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