Michael M. Knott, M.D.
Country not established
- Devices
- 2
What Michael M. Knott, M.D. makes
The manufacturer produces nasal medical devices, including the Nosebleed Noseclip for temporary pressure control during epistaxis and the Knott NG Tube, a nasogastric tube designed for feeding or drainage in clinical settings.
These devices are regulated under Class I and Class II classifications in the U.S. and are listed in the FDA 510(k) registry. The company is based in the United States.
Catalogue
Nosebleed Noseclip Ref K981966
Regimes: 510(k) Registry: 510(k)Knott Ng Tube Ref K971354
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Michael M. Knott, M.D. have in the registry?
The registry currently lists 2 devices for Michael M. Knott, M.D.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Michael M. Knott, M.D.'s devices?
Among its 2 most recently registered devices, Michael M. Knott, M.D. has devices listed in FDA 510(k) (2 devices).
What risk classes do Michael M. Knott, M.D.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Michael M. Knott, M.D.'s devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from Michael M. Knott, M.D. in the registry?
The most recently registered devices listed for Michael M. Knott, M.D. include NOSEBLEED NOSECLIP and KNOTT NG TUBE.