FDA 510(k) Application Details - K024132

Device Classification Name	Light, Surgical, Ceiling Mounted   More FDA Info for this Device
510(K) Number	K024132
Device Name	Light, Surgical, Ceiling Mounted
Applicant	BERCHTOLD HOLDING GMBH LUDWIGSTALER STR. 25 TUTTLINGEN D-78532 DE Other 510(k) Applications for this Company
Contact	JORG SCHNEIDER Other 510(k) Applications for this Contact
Regulation Number	878.4580   More FDA Info for this Regulation Number
Classification Product Code	FSY Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	12/16/2002
Decision Date	03/21/2003
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	SU - General & Plastic Surgery
Review Advisory Committee	SU - General & Plastic Surgery
Statement / Summary / Purged Status	Summary
Type	Special
Reviewed By Third Party	N
Expedited Review