Smith Assoc.
Country not established
- Devices
- 1
What Smith Assoc. makes
Smith Assoc. manufactures the MSI Pressure Infusor, a device designed for controlled infusion of fluids under pressure in medical settings.
The MSI Pressure Infusor is classified as a Class I medical device and is listed under the FDA’s 510(k) pathway. The company is based in the United States.
Catalogue
Msi Pressure Infusor Ref K973843
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Smith Assoc. have in the registry?
The registry currently lists 1 device for Smith Assoc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Smith Assoc.'s devices?
Among its 1 most recently registered device, Smith Assoc. has devices listed in FDA 510(k) (1 device).
What risk classes do Smith Assoc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Smith Assoc.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Smith Assoc. in the registry?
The most recently registered devices listed for Smith Assoc. include MSI PRESSURE INFUSOR.