Airmed Corp.
United StatesFDA applicant, unverified
- Devices
- 3
What Airmed Corp. makes
Airmed Corp. manufactures respiratory support devices, including ventilator tubing for mechanical ventilation, sized-particle aerosol nebulizers for precise medication delivery, and compressor units for nebulizer therapy.
The company’s products are regulated under FDA’s 510(k) pathway, with devices classified as Class I and Class II. These items are listed in the U.S. Food and Drug Administration’s 510(k) database. The manufacturer is based in the United States.
Catalogue
Vent-Well Ventilator Tubing Ref K841378
Regimes: 510(k) Registry: 510(k)Optimist Sized Particle Aerosol Nebuliz Ref K841322
Regimes: 510(k) Registry: 510(k)Air-Neb Nebulizer Compressor Unit Ref K841321
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Airmed Corp. have in the registry?
The registry currently lists 3 devices for Airmed Corp.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Airmed Corp.'s devices?
Among its 3 most recently registered devices, Airmed Corp. has devices listed in FDA 510(k) (3 devices).
What risk classes do Airmed Corp.'s devices fall under?
Among its 3 most recently registered devices, the classes recorded for Airmed Corp.'s devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from Airmed Corp. in the registry?
The most recently registered devices listed for Airmed Corp. include VENT-WELL VENTILATOR TUBING, OPTIMIST SIZED PARTICLE AEROSOL NEBULIZ and AIR-NEB NEBULIZER COMPRESSOR UNIT.