I.P.I. Medical Products
Country not established
- Devices
- 1
What I.P.I. Medical Products makes
I.P.I. Medical Products manufactures the IPI Humidifier Chamber, a device designed for use with respiratory therapy to deliver humidified gases to patients.
The company’s portfolio is regulated under FDA’s Class II designation and requires 510(k) clearance. The device is listed in the FDA’s 510(k) registry. The manufacturer is based in the United States.
Catalogue
Ipi Humidifier Chamber Ref K993282
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does I.P.I. Medical Products have in the registry?
The registry currently lists 1 device for I.P.I. Medical Products. Devices recorded under merged duplicate company entries are counted once.
Which registries list I.P.I. Medical Products's devices?
Among its 1 most recently registered device, I.P.I. Medical Products has devices listed in FDA 510(k) (1 device).
What risk classes do I.P.I. Medical Products's devices fall under?
Among its 1 most recently registered device, the classes recorded for I.P.I. Medical Products's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from I.P.I. Medical Products in the registry?
The most recently registered devices listed for I.P.I. Medical Products include IPI HUMIDIFIER CHAMBER.