Diagnostic Monitoring Software is one of 18590 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Diagnostic Monitoring Software - FDA 510(k) Cleared Devices
Recent clearances: DMS 300-2W HOLTER ECG RECORDER, DMS 300-2, 300-3 AND 300-4, PREMIER 11 HOLTER
5
Total
5
Cleared
0
Denied
Diagnostic Monitoring Software has 5 FDA 510(k) cleared medical devices. Based in Tustin, US.
Historical record: 5 cleared submissions from 1992 to 2014. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Diagnostic Monitoring Software Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Diagnostic Monitoring Software
5 devices
Cleared
May 19, 2014
DMS 300-2W HOLTER ECG RECORDER
Cardiovascular
236d
Cleared
Oct 16, 2006
DMS 300-2, 300-3 AND 300-4
Cardiovascular
17d
Cleared
Aug 25, 2006
PREMIER 11 HOLTER
Cardiovascular
32d
Cleared
Aug 16, 2006
DMS 300-7
Cardiovascular
30d
Cleared
Jan 08, 1992
HOLTER 24-HOUR ECG SYSTEM, MODEL NUMBER: DMS 300
Cardiovascular
272d