FDA 510(k) Applications Submitted by SHAWN RIEDEL

FDA 510(k) Number	Submission Date	Device Name	Applicant
K100047	01/08/2010	SUREFIT DUAL DISPERSIVE ELECTRODE	CONMED CORPORATION
K120322	02/02/2012	CONMED SUREFIT DUAL DISPERSIVE ELECTRODE	CONMED CORPORATION
K120476	02/16/2012	MACROLYTE DISPERSIVE ELECTRODE	CONMED CORPORATION
K100686	03/10/2010	CONMED MACROLYTE DISPERSIVE ELECTRODE	CONMED CORPORATION
K021830	06/04/2002	SORIN BIOMEDICA SMARXT BCD VANGUARD SURFACE MODIFIED CARDIOPLEGIA SYSTEM	COBE CARDIOVASCULAR, INC.
K081634	06/11/2008	CONMED GOLDVAC INTEGRATED SMOKE EVACUATION PENCIL	CONMED CORPORATION
K022321	07/17/2002	STOCKERT V172-28 VENOUS FEMORAL CANNULA	STOCKERT INSTRUMENTE GMBH
K062082	07/21/2006	CONMED ABC DISSECTING BLADE ELECTRODE, MODEL 139330; BLUNT NEEDLE ELECTRODE, MODEL 139331	CONMED CORPORATION
K013480	10/19/2001	COBE SMARXT OPTIMIN SURFACE MODIFIED HOLLOW FIBER MEMBRANE OXYGENATOR	COBE CARDIOVASCULAR, INC.
K013915	11/27/2001	D902 PH.I.S.I.O OXYGENATOR; D920 PH.I.S.I.O RESERVOIR; DIDECO D736 PH.I.S.I.O FILTER	DIDECO S.P.A.
K103665	12/16/2010	CONMED R SABRE GENESIS TM ELECTROSURGICAL UNIT; CONED R SABRE GENESIS TM ELECTROSURGICAL UNIT (230V); CONMED HYFRESURG O	CONMED CORPORATION