Meridian Dynamics Biomedical, Inc.
Country not established
- Devices
- 1
What Meridian Dynamics Biomedical, Inc. makes
Meridian Dynamics Biomedical, Inc. manufactures the ECG PEN, a handheld device designed for electrocardiogram (ECG) recording and analysis.
The ECG PEN is classified as a Class II medical device under FDA regulations and is listed in the FDA’s 510(k) clearance registry. The company is based in the United States.
Catalogue
Ecg Pen Ref K103077
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Meridian Dynamics Biomedical, Inc. have in the registry?
The registry currently lists 1 device for Meridian Dynamics Biomedical, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Meridian Dynamics Biomedical, Inc.'s devices?
Among its 1 most recently registered device, Meridian Dynamics Biomedical, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Meridian Dynamics Biomedical, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Meridian Dynamics Biomedical, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Meridian Dynamics Biomedical, Inc. in the registry?
The most recently registered devices listed for Meridian Dynamics Biomedical, Inc. include ECG PEN.