FDA 510(k) Application Details - K131839

Device Classification Name	Powered Laser Surgical Instrument   More FDA Info for this Device
510(K) Number	K131839
Device Name	Powered Laser Surgical Instrument
Applicant	DC INTERNATIONAL, LLC 624 CYPRESS GREEN CIR. WELLINGTON, FL 33414 US Other 510(k) Applications for this Company
Contact	DAVID BOEGLER Other 510(k) Applications for this Contact
Regulation Number	878.4810   More FDA Info for this Regulation Number
Classification Product Code	GEX Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	06/21/2013
Decision Date	11/07/2013
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	N
Expedited Review