FDA 510(k) Application Details - K960196

Device Classification Name	Table, Powered   More FDA Info for this Device
510(K) Number	K960196
Device Name	Table, Powered
Applicant	TRI W-G, INC. 215 12TH AVE., N.E. P.O. BOX 905 VALLEY CITY, ND 58072 US Other 510(k) Applications for this Company
Contact	DAVID KESLER Other 510(k) Applications for this Contact
Regulation Number	890.3760   More FDA Info for this Regulation Number
Classification Product Code	INQ Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	01/16/1996
Decision Date	02/07/1996
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	PM - Physical Medicine
Review Advisory Committee	PM - Physical Medicine
Statement / Summary / Purged Status	Summary
Type	Traditional
Reviewed By Third Party	N
Expedited Review