Impulse Systems, Inc.
Country not established
- Devices
- 1
What Impulse Systems, Inc. makes
Impulse Systems, Inc. manufactures the Impulse Epidural Electrode, a device designed for epidural stimulation applications in neurological and pain management therapies.
The company’s portfolio is regulated under FDA Class II devices and listed via the 510(k) clearance pathway. The manufacturer is based in the United States.
Catalogue
Impulse Epidural Electrode Ref K884663
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Impulse Systems, Inc. have in the registry?
The registry currently lists 1 device for Impulse Systems, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Impulse Systems, Inc.'s devices?
Among its 1 most recently registered device, Impulse Systems, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Impulse Systems, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Impulse Systems, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Impulse Systems, Inc. in the registry?
The most recently registered devices listed for Impulse Systems, Inc. include IMPULSE EPIDURAL ELECTRODE.