FDA 510(k) Applications Submitted by Brian Kunst

FDA 510(k) Number	Submission Date	Device Name	Applicant
K080451	02/19/2008	UNIBLATE ELECTROSURGICAL DEVICE	ANGIODYNAMICS, INC.
K971314	04/09/1997	DCAT EMBOLECTOMY CATHETER SYSTEM	ANGIODYNAMICS, INC.
K161134	04/22/2016	Bovie Bantam/PRO Electrosurgical Generator, Bovie DERM 941 Electrosurgical Generator, Bovie DERM 942 Electrosurgical Generator	BOVIE MEDICAL CORPORATION
K961763	05/07/1996	PULSE*SPRAY INFUSION SYSTEM	ANGIODYNAMICS, DIV. E-Z-EM, INC.
K151325	05/18/2015	Bovie J-Plasma Handpiece	BOVIE MEDICAL CORPORATION
K081472	05/27/2008	SMARTPORT CT VORTEX; LP TITANIUM, SINGLE PLASTIC, SINGLE TITANIUM, TRIUMPH LOW PROFILE TITANIUM PORTS	ANGIODYNAMICS, INC.
K982346	07/06/1998	ANGIODYNAMICS ANGIOSTENT BILIARY STENT SYSTEM	ANGIODYNAMICS, INC.
K092486	08/13/2009	VORTEX MEDICAL ANGIOVAC CARDIOPULMONARY BYPASS CIRCUIT	VORTEX MEDICAL INC
K953825	08/15/1995	ANGIOFLUSH II FLUID MANAGEMENT SYSTEM	ANGIODYNAMICS, INC.
K072375	08/23/2007	SMARTPORT CT MP PORT ACCESS SYSTEM AND LIFEGUARD CT SAFETY INFUSION SET	ANGIODYNAMICS, INC.
K152570	09/09/2015	Bovie J-Plasma Precise 360 Handpiece	BOVIE MEDICAL CORPORATION
K102762	09/24/2010	ORTHOSTAT BONE HEMOSTAT MATRIX APPLICATOR	ORTHOCON, INC.
K152777	09/25/2015	Bovie Disposable Bipolar Ablator	BOVIE MEDICAL CORPORATION
K964033	10/08/1996	3F ANGIOPTIC ANGIOGRAPHIC CATHETER	ANGIODYNAMICS, INC.
K964034	10/08/1996	TRANSJUGULAR ACCESS SET	ANGIODYNAMICS, INC.