Gsi Medical Systems
Country not established
- Devices
- 1
What Gsi Medical Systems makes
Gsi Medical Systems manufactures the MICROAIR PUP, a portable, battery-powered microinfusion pump designed for continuous, precise delivery of fluids in medical settings.
The MICROAIR PUP is classified as a Class II device under FDA regulations and is listed in the FDA’s 510(k) clearance registry. The company is based in the United States.
Catalogue
Microair Pup Ref K925694
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Gsi Medical Systems have in the registry?
The registry currently lists 1 device for Gsi Medical Systems. Devices recorded under merged duplicate company entries are counted once.
Which registries list Gsi Medical Systems's devices?
Among its 1 most recently registered device, Gsi Medical Systems has devices listed in FDA 510(k) (1 device).
What risk classes do Gsi Medical Systems's devices fall under?
Among its 1 most recently registered device, the classes recorded for Gsi Medical Systems's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Gsi Medical Systems in the registry?
The most recently registered devices listed for Gsi Medical Systems include MICROAIR PUP.