Diagnostic Monitoring
Country not established
- Devices
- 1
What Diagnostic Monitoring makes
The company manufactures the DM-400 Holter ECG cassette recorder, a portable device designed for continuous ambulatory electrocardiographic monitoring to record heart rhythms over extended periods.
This device is classified as Class II under FDA regulations and is listed in the 510(k) clearance registry. The company is based in the United States.
Catalogue
Dm-400 Holter Ecg Cassette Recorder Ref K970298
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Diagnostic Monitoring have in the registry?
The registry currently lists 1 device for Diagnostic Monitoring. Devices recorded under merged duplicate company entries are counted once.
Which registries list Diagnostic Monitoring's devices?
Among its 1 most recently registered device, Diagnostic Monitoring has devices listed in FDA 510(k) (1 device).
What risk classes do Diagnostic Monitoring's devices fall under?
Among its 1 most recently registered device, the classes recorded for Diagnostic Monitoring's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Diagnostic Monitoring in the registry?
The most recently registered devices listed for Diagnostic Monitoring include DM-400 HOLTER ECG CASSETTE RECORDER.