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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