FDA 510(k) Applications Submitted by CHELSEA PIOSKE

FDA 510(k) Number	Submission Date	Device Name	Applicant
K191305	05/14/2019	Hereaeus Poseidon Microcatheter	Heraeus Medical Components, LLC
K191502	06/06/2019	Heraeus Peripheral Guidewire	Heraeus Medical Components, LLC
K132645	08/23/2013	THORATRAK MICS RETRACTOR SYSTEM, RACK, BLADES	MEDTRONIC, INC.
K132995	09/24/2013	DLP RETROGRADE CORONARY SINUS PERFUSION CANNULA WITHOUT PRESSURE MONITORING LINE, DLP RETROGRADE CORONARY SINUS PERFUSIO	MEDTRONIC INC.
K123762	12/07/2012	DLP RETROGRADE CORONARY SINUS PERFUSION CANNULA WITH AUTO-INFLATE CUFF	MEDTRONIC INC.
K150422	02/19/2015	EOPA 3D Arterial Cannula	MEDTRONIC, INC.
K151110	04/27/2015	Intersept Filtered Cardiotomy Reservoir	Medtronic, Inc