Monebo Technologies, Inc.
United StatesFDA applicant, unverified
- Devices
- 3
What Monebo Technologies, Inc. makes
Monebo Technologies, Inc. develops software libraries for automated cardiac analysis, including algorithms for arrhythmia detection and ECG interpretation, as well as disposable electrode belts for electrocardiogram monitoring.
These products are classified as Class II medical devices under FDA regulations and are listed via the 510(k) pathway. The company is based in the United States.
Catalogue
- Regimes: 510(k) Registry: 510(k)
- Regimes: 510(k) Registry: 510(k)
Cardiobelt Electrode Belt Ref K063044
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Monebo Technologies, Inc. have in the registry?
The registry currently lists 3 devices for Monebo Technologies, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Monebo Technologies, Inc.'s devices?
Among its 3 most recently registered devices, Monebo Technologies, Inc. has devices listed in FDA 510(k) (3 devices).
What risk classes do Monebo Technologies, Inc.'s devices fall under?
Among its 3 most recently registered devices, the classes recorded for Monebo Technologies, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Monebo Technologies, Inc. in the registry?
The most recently registered devices listed for Monebo Technologies, Inc. include MONEBO AUTOMATIC ARRHYTHMIA DETECTION SOFTWARE LIBRARY, VERSION 1, MONEBO AUTOMATED ECG ANALYSIS AND INTERPRETATION SOFTWARE LIBRARY, VERSION 3.0 and CARDIOBELT ELECTRODE BELT.