FDA 510(k) Applications Submitted by MARK MURPHY

FDA 510(k) Number	Submission Date	Device Name	Applicant
K140329	02/10/2014	RENEGADE HI-FLO MICROCATHETER, MICROCATHETER KIT, FATHOM SYSTEM, FATHOM KIT	BOSTON SCIENTIFIC
K980859	03/05/1998	HEMOCOR HPH MINI HEMOCONCENTRATOR	MINNTECH CORP.
K200583	03/06/2020	Ki Mobility Focus CR, Ki Mobility Focus CRe, Ki Mobility Focus CR TTL	Ki Mobility LLC
K080982	04/07/2008	STERLING ES MONORAIL AND OVER-THE-WIRE PTA BALLOON DILATATION CATHETERS	BOSTON SCIENTIFIC CORP.
K111295	05/10/2011	.014 MONORAIL AND OTW PTA BALLOON DILATATION CATHETERS	Boston Scientific Corporation
K201869	07/07/2020	Ki Power Tilt System	Ki Mobility LLC
K983085	09/03/1998	HEMOCOR HPH 700 HEMOCONCENTRATOR	MINNTECH CORP.
K983126	09/08/1998	FIBERFLO HOLLOW FIBER CAPSULE WATER FILTERS	MINNTECH CORP.
K223527	11/23/2022	Little Wave Clik, Rogue XP, Little Wave XP, Spark	Ki Mobility LLC
K223533	11/23/2022	Little Wave Arc; Little Wave Flip	Ki Mobility LLC
K093720	12/02/2009	STERLING SL MONORAIL PTA BALLOON DILATATION CATHETERS STERLING SL OVER-THE-WIRE BALLOON DILATATION CATHETERS MODEL VARIO	BOSTON SCIENTIFIC CORP.
K014195	12/21/2001	KAYAK HYDROPHILIC GUIDE WIRES	BOSTON SCIENTIFIC CORP.