FDA 510(k) Applications Submitted by Susan Kagan

FDA 510(k) Number Submission Date Device Name Applicant
K120095 01/12/2012 SIDE EFFECT WITH HAND CONTROLS, HOOK ELECTRODE WITH HAND CONTROLS, 2.3 WEDGE ELECTRODE WITH HAND CONTROLS, S90 WITH HAND DEPUY MITEK, A JOHNSON & JOHNSON COMPANY
K130169 01/24/2013 FMS VUE FLUID MANAGMENT SYSTEM, FMS CONNECT INTERFACE CABLE DEPUY MITEK, A JOHNSON & JOHNSON COMPANY
K100638 03/05/2010 VAPR VUE RADIOFREQUENCY SYSTEM ,MODEL 225024, VPR VUE WIRELESS FOOTSWITCH, MODEL 227214 DEPUY MITEK, A JOHNSON & JOHNSON COMPANY
K140896 04/08/2014 VAPR ARCTIC SUCTION ELECTRODE DEPUY MITEK, A JOHNSON & JOHNSON COMPANY
K131191 04/26/2013 4MM & 5MM FULL RADIUS BLADE PLUS, 4MM & 5MM BARREL BUR PLUS/4MM BARREL TORNADO BUR PLUS, 4MM & 5MM AGGRESSIVE BLADE PLUS DEPUY MITEK, A JOHNSON & JOHNSON COMPANY
K061876 07/03/2006 CODMAN VPV SYSTEM, MODEL 82-3192 Codman & Shurtleff, Inc.
K053107 11/04/2005 CODMAN HAKIM PROGRAMMABLE VALVE W/WO SIPHONGUARD Codman & Shurtleff, Inc.
K043258 11/24/2004 MODIFIED TFX MEDICAL SAFETY NEEDLE WITH INTRODUCER, PART NO. T4634-02 TELEFLEX MEDICAL
K113545 12/01/2011 VAPR VUE GENERATOR, VAPR 3 ELECTROSURGICAL SYSTEM, VAPR II ELECTROSURGICAL SYSTEM COOLPLUSE 90 AND COOLPLUSE 90 WITH HAN DEPUY MITEK, A JOHNSON & JOHNSON COMPANY
K143475 12/05/2014 VAPR Tripolar Suction Electrode Depuy Mitek
K133941 12/23/2013 MITEK ARTHROSCOPES MEDOS INTERNATIONAL SARL


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