Copd Partners, Inc.
United StatesFDA applicant, unverified
- Devices
- 2
What Copd Partners, Inc. makes
Copd Partners, Inc. manufactures portable and home-use liquid oxygen systems, including the Model 300P for patient mobility and the Model 300D for stationary home oxygen therapy.
These devices are classified as Class II under FDA regulations and are listed via the 510(k) pathway. The company is based in the United States.
Catalogue
Copd Liquid Oxygen Portable, Model 300P Ref K072011
Regimes: 510(k) Registry: 510(k)Model 300D Home Oxygen Liquefier Ref K071461
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Copd Partners, Inc. have in the registry?
The registry currently lists 2 devices for Copd Partners, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Copd Partners, Inc.'s devices?
Among its 2 most recently registered devices, Copd Partners, Inc. has devices listed in FDA 510(k) (2 devices).
What risk classes do Copd Partners, Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Copd Partners, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Copd Partners, Inc. in the registry?
The most recently registered devices listed for Copd Partners, Inc. include COPD LIQUID OXYGEN PORTABLE, MODEL 300P and MODEL 300D HOME OXYGEN LIQUEFIER.