Neuro Supplies, Inc.
United StatesFDA applicant, unverified
- Devices
- 5
What Neuro Supplies, Inc. makes
Neuro Supplies, Inc. manufactures reusable and disposable cutaneous electrodes, including disc, bar, and ground types, as well as specialized surface electrodes for EEG, EP, and EMG monitoring. Their product line includes digital ring electrodes designed for specific physiological signal detection. These devices are intended for temporary skin attachment in clinical and research settings.
The company’s electrodes are classified as Class II medical devices under FDA regulations and are supported by 510(k) clearance records. Their products are listed in the FDA’s 510(k) database. The manufacturer operates from the United States.
Catalogue
Cutaneous (Disc) Electrode Ref K991772
Regimes: 510(k) Registry: 510(k)Digital Ring Electrde Ref K991771
Regimes: 510(k) Registry: 510(k)Cutaneous (Bar) Electrode Ref K991769
Regimes: 510(k) Registry: 510(k)Cutaneous (Ground) Electrode Ref K991770
Regimes: 510(k) Registry: 510(k)Neurolink Eeg/Ep/Emg Surface Electrodes Ref K942921
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Neuro Supplies, Inc. have in the registry?
The registry currently lists 5 devices for Neuro Supplies, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Neuro Supplies, Inc.'s devices?
Among its 5 most recently registered devices, Neuro Supplies, Inc. has devices listed in FDA 510(k) (5 devices).
What risk classes do Neuro Supplies, Inc.'s devices fall under?
Among its 5 most recently registered devices, the classes recorded for Neuro Supplies, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Neuro Supplies, Inc. in the registry?
The most recently registered devices listed for Neuro Supplies, Inc. include CUTANEOUS (DISC) ELECTRODE, DIGITAL RING ELECTRDE, CUTANEOUS (BAR) ELECTRODE and CUTANEOUS (GROUND) ELECTRODE.