Memory MD, Inc.
United StatesFDA applicant, unverified
- Devices
- 3
What Memory MD, Inc. makes
Memory MD, Inc. manufactures neurophysiological monitoring systems, including NeuroEEG devices and NeuroCap (Model DEC22) for electrophysiological recording. These tools are designed for capturing and analyzing brain activity data in clinical settings.
The company’s portfolio is regulated under FDA Class II devices, with products authorised via the 510(k) pathway. These devices are listed in the FDA’s 510(k) registry. The manufacturer is based in the United States.
Catalogue
NeuroEEG Ref K173460
Regimes: 510(k) Registry: 510(k)NeuroCap (Model DEC22) Ref K202913
Regimes: 510(k) Registry: 510(k)NeuroCap Ref K172866
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Memory MD, Inc. have in the registry?
The registry currently lists 3 devices for Memory MD, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Memory MD, Inc.'s devices?
Among its 3 most recently registered devices, Memory MD, Inc. has devices listed in FDA 510(k) (3 devices).
What risk classes do Memory MD, Inc.'s devices fall under?
Among its 3 most recently registered devices, the classes recorded for Memory MD, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Memory MD, Inc. in the registry?
The most recently registered devices listed for Memory MD, Inc. include NeuroEEG, NeuroCap (Model DEC22) and NeuroCap.