FDA 510(k) Applications Submitted by PAUL SUMNER

FDA 510(k) Number Submission Date Device Name Applicant
K070248 01/25/2007 VELOCITYAIS VELOCITY MEDICAL SOLUTIONS, LLC
K070550 02/27/2007 AUSCO ES-3100 KORATEK COMPANY, LTD.
K140909 04/09/2014 MCKESSON RADIOLOGY MCKESSON MEDICAL IMAGING COMPANY
K081076 04/16/2008 VELOCITYAIS, VELOCITY AI, VELOCITYVX, VELOCITYRT, V-RESPONSE VELOCITY MEDICAL SOLUTIONS, LLC
K101109 04/20/2010 VIVATRAK WIRELESS MEDCARE, LLC
K111149 04/25/2011 HANAROSTENT BILIARY (NNN) M.I. TECH CO., LTD.
K131497 05/24/2013 MCKESSON CARDIOLOGY HEMO MCKESSON ISRAEL LTD.
K101838 07/01/2010 VTS1000 VUETEK SCIENTIFIC LLC
K002240 07/24/2000 RENDER-PLAN 3-D 4.00 & PRECISE-PLAN 1.0 PRECISION THERAPY INTL., INC.
K072259 08/14/2007 OPHTHALMOSCOPE F-10 NIDEK CO., LTD.
K112457 08/26/2011 LEFORTE SYSTEM BONE PLATE & SCREW ARKIN CONSULTING GROUP
K112812 09/27/2011 LEFORTE NEURO SYSTEM BONE PLATE JEIL MEDICAL CORPORATION
K133534 11/18/2013 MCKESSON CARDIOLOGY ECG MOBILE MCKESSON ISRAEL LTD.
K103778 12/27/2010 LEFORTE NEURO SYSTEM BONE PLATE JEIL MEDICAL CORPORATION
K981790 05/20/1998 IVIEW ELECTRONIC PORTAL IMAGING DEVICE (EPID) MODEL NUMBER IVEW ELEKTA ONCOLOGY SYSTEMS, LTD.
K982713 08/04/1998 RT DESKTOP ELEKTA ONCOLOGY SYSTEMS, LTD.
K983678 10/20/1998 ELEKTA ONCOLOGY SYSTEMS PRECISE TREATMENT TABLE ELEKTA INSTRUMENTS, INC.


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