Telemed Div.
Country not established
- Devices
- 2
What Telemed Div. makes
Telemed Div. manufactures electrocardiograph devices, including the OMNIGRAPH 4000 and OMNIGRAPH 6000 models, designed for recording and analyzing heart electrical activity.
These devices are classified as Class II under FDA regulations and are listed in the 510(k) clearance registry. The company is based in the United States.
Catalogue
Omnigraph 4000(Electrocardiograph) Ref K852652
Regimes: 510(k) Registry: 510(k)Omnigraph 6000 Ref K880357
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Telemed Div. have in the registry?
The registry currently lists 2 devices for Telemed Div.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Telemed Div.'s devices?
Among its 2 most recently registered devices, Telemed Div. has devices listed in FDA 510(k) (2 devices).
What risk classes do Telemed Div.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Telemed Div.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Telemed Div. in the registry?
The most recently registered devices listed for Telemed Div. include OMNIGRAPH 4000(ELECTROCARDIOGRAPH) and OMNIGRAPH 6000.