FDA 510(k) Application Details - K042382

Device Classification Name	Light, Surgical, Ceiling Mounted   More FDA Info for this Device
510(K) Number	K042382
Device Name	Light, Surgical, Ceiling Mounted
Applicant	MED-GENERAL TECHNOLOGIES LLC 1016 COLLIER CENTER WAY SUITE 102 NAPLES, FL 34110 US Other 510(k) Applications for this Company
Contact	PAUL MCCREIGHT 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	09/01/2004
Decision Date	11/30/2004
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