FDA 510(k) Application Details - K072904

Device Classification Name	Instrument, Ultrasonic Surgical   More FDA Info for this Device
510(K) Number	K072904
Device Name	Instrument, Ultrasonic Surgical
Applicant	SOERING GMBH 1600 MANCHESTER WAY CORINTH, TX 76210 US Other 510(k) Applications for this Company
Contact	CARL THOMAS Other 510(k) Applications for this Contact
Regulation Number	000.0000   More FDA Info for this Regulation Number
Classification Product Code	LFL Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	10/11/2007
Decision Date	05/21/2008
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	-
Review Advisory Committee	SU - General & Plastic Surgery
Statement / Summary / Purged Status	Summary
Type	Traditional
Reviewed By Third Party	N
Expedited Review