Datrix is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Datrix - FDA 510(k) Cleared Devices
5
Total
5
Cleared
0
Denied
Datrix has 5 FDA 510(k) cleared medical devices. Based in Escondido, US.
Historical record: 5 cleared submissions from 1992 to 2005. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Datrix Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Datrix
5 devices
Cleared
Nov 30, 2005
DATRIX CARDIO WIFI ELECTROCARDIOGRAPH
Cardiovascular
28d
Cleared
Nov 01, 2005
CARDIOSERVER
Cardiovascular
19d
Cleared
Oct 15, 2003
DIGITAL AMBULATORY ECG (HOLTER) RECORDER
Cardiovascular
194d
Cleared
Nov 10, 1998
DIGITAL ECG HOLTER RECORDER, MODEL DR512
Cardiovascular
76d
Cleared
Mar 30, 1992
GIKTER ECG CASSETTE TAPE RECORDER MODEL XR 300
Cardiovascular
24d