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FDA 510(k) Applications Submitted by DATRIX
FDA 510(k) Number
Submission Date
Device Name
Applicant
K982975
08/26/1998
DIGITAL ECG HOLTER RECORDER, MODEL DR512
DATRIX
K031074
04/04/2003
DIGITAL AMBULATORY ECG (HOLTER) RECORDER
DATRIX
K052883
10/13/2005
CARDIOSERVER
DATRIX
K053083
11/02/2005
DATRIX CARDIO WIFI ELECTROCARDIOGRAPH
DATRIX
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