Diagnostic Monitoring Software
Country not established
- Devices
- 5
What Diagnostic Monitoring Software makes
The company manufactures diagnostic monitoring software and hardware systems focused on Holter ECG recording and 24-hour ambulatory cardiac monitoring. Products include standalone Holter ECG recorders, such as the DMS 300-2W and DMS 300 series, as well as integrated systems like the PREMIER 11 Holter and the DMS 300-7 for continuous cardiac rhythm analysis.
These devices are classified as Class II under FDA regulations and are authorised through the 510(k) clearance process. The portfolio is listed in the FDA’s 510(k) database, and the company operates from the United States.
Catalogue
Dms 300-7 Ref K062007
Regimes: 510(k) Registry: 510(k)Premier 11 Holter Ref K062088
Regimes: 510(k) Registry: 510(k)Dms 300-2W Holter Ecg Recorder Ref K133014
Regimes: 510(k) Registry: 510(k)Holter 24-Hour Ecg System, Model Number: Dms 300 Ref K911615
Regimes: 510(k) Registry: 510(k)Dms 300-2, 300-3 And 300-4 Ref K062959
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Diagnostic Monitoring Software have in the registry?
The registry currently lists 5 devices for Diagnostic Monitoring Software. Devices recorded under merged duplicate company entries are counted once.
Which registries list Diagnostic Monitoring Software's devices?
Among its 5 most recently registered devices, Diagnostic Monitoring Software has devices listed in FDA 510(k) (5 devices).
What risk classes do Diagnostic Monitoring Software's devices fall under?
Among its 5 most recently registered devices, the classes recorded for Diagnostic Monitoring Software's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Diagnostic Monitoring Software in the registry?
The most recently registered devices listed for Diagnostic Monitoring Software include DMS 300-7, PREMIER 11 HOLTER, DMS 300-2W HOLTER ECG RECORDER and HOLTER 24-HOUR ECG SYSTEM, MODEL NUMBER: DMS 300.