Andromeda Research, Inc.
Country not established
- Devices
- 1
What Andromeda Research, Inc. makes
Andromeda Research, Inc. manufactures the Pulsar Neurostimulator, a neurostimulation device intended for therapeutic use.
The Pulsar Neurostimulator is classified as a Class II medical device and is listed in the FDA 510(k) registry. Andromeda Research is based in the United States.
Catalogue
Pulsar Neurostimulator Ref K852061
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Andromeda Research, Inc. have in the registry?
The registry currently lists 1 device for Andromeda Research, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Andromeda Research, Inc.'s devices?
Among its 1 most recently registered device, Andromeda Research, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Andromeda Research, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Andromeda Research, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Andromeda Research, Inc. in the registry?
The most recently registered devices listed for Andromeda Research, Inc. include PULSAR NEUROSTIMULATOR.