FDA 510(k) Application Details - K955750

Device Classification Name	Table, Operating-Room, Ac-Powered   More FDA Info for this Device
510(K) Number	K955750
Device Name	Table, Operating-Room, Ac-Powered
Applicant	BERCHTOLD HOLDING GMBH LUDWIGSTALER STR. 25 TUTTLINGEN D-78532 DE Other 510(k) Applications for this Company
Contact	WOLFRAM K HILL Other 510(k) Applications for this Contact
Regulation Number	878.4960   More FDA Info for this Regulation Number
Classification Product Code	FQO Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	12/18/1995
Decision Date	02/08/1996
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	SU - General & Plastic Surgery
Review Advisory Committee	SU - General & Plastic Surgery
Statement / Summary / Purged Status	Statement
Type	Traditional
Reviewed By Third Party	N
Expedited Review