FDA 510(k) Applications Submitted by JAMES LUKER

FDA 510(k) Number Submission Date Device Name Applicant
K160057 01/12/2016 ArcCHECK-MR Sun Nuclear Corporation
K150848 03/31/2015 Dose Calculator SUN NUCLEAR CORPORATION
K101571 06/04/2010 XPER INFORMATION MANAGEMENT AND FLEX CARDIO PHYSIOMONITORING SYSTEMS WITT BIOMEDICAL CORP
K142142 08/05/2014 QUALITY REPORTS SUN NUCLEAR CORPORATION
K063547 11/24/2006 CALYSTO SERIES IV PHYSIO-MONITORING AND INFORMATION SYSTEM WITT BIOMEDICAL CORP
K063840 12/26/2006 XPER INFORMATION MANAGEMENT/PHYSIOMONITORING 5 SYSTEM AND/OR VASCULAR 5, PATIENT CARE CONSOLE AND CENTRAL STATION WITT BIOMEDICAL CORP


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