FDA 510(k) Application Details - K970807

Device Classification Name	Table, Operating-Room, Electrical   More FDA Info for this Device
510(K) Number	K970807
Device Name	Table, Operating-Room, Electrical
Applicant	STIERLEN-MAQUET AG P.O. BOX 2162 RASTATT 76411 DE Other 510(k) Applications for this Company
Contact	REINHARD PFEUFFER Other 510(k) Applications for this Contact
Regulation Number	878.4960   More FDA Info for this Regulation Number
Classification Product Code	GDC Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	03/05/1997
Decision Date	03/14/1997
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	SU - General & Plastic Surgery
Review Advisory Committee	SU - General & Plastic Surgery
Statement / Summary / Purged Status	Summary
Type	Traditional
Reviewed By Third Party	Y
Expedited Review