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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.
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