FDA 510(k) Applications Submitted by Doug Atkins

FDA 510(k) Number	Submission Date	Device Name	Applicant
K090253	02/02/2009	ANGIOJET ULTRA DVX THROMBECTOMY SET, MODEL 106552-001, ANGIOJET ULTRA XPEEDIOR THROMBECTOMY SET, MODEL 105040-001	POSSIS MEDICAL, INC.
K040568	03/04/2004	POLYETHER URETHANE MATERIAL CHANGE IN NEUROSTIMULATION LEADS	MEDTRONIC VASCULAR
K111182	04/27/2011	ANGIOJET SOLENT OMNI THROMBECTOMY SET	MEDRAD, INC.
K101354	05/14/2010	FETCH 2 ASPIRATION CATHETER MODEL 109400-001	MEDRAD INTERVENTIONAL/POSSIS
K101406	05/19/2010	ANGIOJET SOLENT PROXI THROMBECTOMY SET MODEL 109676-001	MEDRAD INTERVENTIONAL/POSSIS
K091593	06/02/2009	ANGIO JET ULTRA DVX AND XPEEDIOR THROMBECTOMY SETS	POSSIS MEDICAL, INC.