Samuel Neff M.D.
Country not established
- Devices
- 1
What Samuel Neff M.D. makes
Samuel Neff M.D. manufactures the SHUNTCHECK (PROMETHEUS 1), a Class II medical device.
The device is regulated under the U.S. FDA 510(k) pathway and is listed in the FDA 510(k) registry; the company is based in the United States.
Catalogue
Shuntcheck (Prometheus 1) Ref K040021
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Samuel Neff M.D. have in the registry?
The registry currently lists 1 device for Samuel Neff M.D.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Samuel Neff M.D.'s devices?
Among its 1 most recently registered device, Samuel Neff M.D. has devices listed in FDA 510(k) (1 device).
What risk classes do Samuel Neff M.D.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Samuel Neff M.D.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Samuel Neff M.D. in the registry?
The most recently registered devices listed for Samuel Neff M.D. include SHUNTCHECK (PROMETHEUS 1).