Moberg Medical, Inc.
United StatesFDA applicant, unverified
- Devices
- 2
What Moberg Medical, Inc. makes
Moberg Medical, Inc. manufactures neurodiagnostic devices, including the NEUROTRAC II system and electroencephalography (EEG) equipment. These products are designed for recording and analyzing electrical activity in the brain, supporting clinical and research applications in neurology.
The company’s portfolio is regulated under FDA Class II devices, with products listed via the 510(k) clearance pathway. These devices are intended for use in the United States.
Catalogue
Neurotrac Ii Ref K914571
Regimes: 510(k) Registry: 510(k)Electroencephalograph (Eeg) Ref K960170
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Moberg Medical, Inc. have in the registry?
The registry currently lists 2 devices for Moberg Medical, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Moberg Medical, Inc.'s devices?
Among its 2 most recently registered devices, Moberg Medical, Inc. has devices listed in FDA 510(k) (2 devices).
What risk classes do Moberg Medical, Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Moberg Medical, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Moberg Medical, Inc. in the registry?
The most recently registered devices listed for Moberg Medical, Inc. include NEUROTRAC II and ELECTROENCEPHALOGRAPH (EEG).