Aa Neuromed Corp.
CanadaFDA applicant, unverified
- Devices
- 1
What Aa Neuromed Corp. makes
Aa Neuromed Corp. manufactures electroanalgesic delivery systems designed to provide neuromodulation for pain management, including transcutaneous electrical nerve stimulation (TENS) and related therapeutic devices.
These devices are classified as Class II under FDA regulations and are authorised via the 510(k) pathway. The company is based in the United States.
Catalogue
Neuromed Electroanalgesic Delivery Systems Ref K083250
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Aa Neuromed Corp. have in the registry?
The registry currently lists 1 device for Aa Neuromed Corp.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Aa Neuromed Corp.'s devices?
Among its 1 most recently registered device, Aa Neuromed Corp. has devices listed in FDA 510(k) (1 device).
What risk classes do Aa Neuromed Corp.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Aa Neuromed Corp.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Aa Neuromed Corp. in the registry?
The most recently registered devices listed for Aa Neuromed Corp. include NEUROMED ELECTROANALGESIC DELIVERY SYSTEMS.