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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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