Pulmonox Medical, Inc.
CanadaFDA applicant, unverified
- Devices
- 3
What Pulmonox Medical, Inc. makes
Pulmonox Medical, Inc. manufactures portable and transportable aerosol delivery systems, including the AERONOX Universal, AERONOX Bedside, and AERONOX Transport models for administering inhaled medications. The company also produces the VIANOX Delivery System in two models (I and II), designed for precise aerosolized drug administration.
These devices are classified as Class II under FDA regulations and are listed via 510(k) clearance. The company is based in the United States.
Catalogue
- Regimes: 510(k) Registry: 510(k)
Vianox Delivery System, Model Ii Ref K033779
Regimes: 510(k) Registry: 510(k)Vianox Delivery System, Model I Ref K023014
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Pulmonox Medical, Inc. have in the registry?
The registry currently lists 3 devices for Pulmonox Medical, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Pulmonox Medical, Inc.'s devices?
Among its 3 most recently registered devices, Pulmonox Medical, Inc. has devices listed in FDA 510(k) (3 devices).
What risk classes do Pulmonox Medical, Inc.'s devices fall under?
Among its 3 most recently registered devices, the classes recorded for Pulmonox Medical, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Pulmonox Medical, Inc. in the registry?
The most recently registered devices listed for Pulmonox Medical, Inc. include AERONOX UNIVERSAL, MODEL P/N 360000, AERONOX BEDSIDE, MODEL P/N 360001, AERONOX TRANSPORT TRANSPORT, MODEL P/N 360002, VIANOX DELIVERY SYSTEM, MODEL II and VIANOX DELIVERY SYSTEM, MODEL I.