Travomed, Inc.
United StatesFDA applicant, unverified
- Devices
- 4
What Travomed, Inc. makes
Travomed, Inc. manufactures portable nebulizer systems, including the TRAVONEB Model # TONE 1 for aerosolized medication delivery, and the TRAVELPAK models (AC-102 and DC-202) for compressed-air and battery-powered operation. The company also produces mechanical oxygen regulators designed for portable oxygen therapy.
These devices are classified as Class II under FDA regulations and are supported by 510(k) clearance records. Travomed, Inc. is based in the United States.
Catalogue
Travoneb Model # Tone 1 Ref K854747
Regimes: 510(k) Registry: 510(k)Travelpak Model Ac-102 Ref K854509
Regimes: 510(k) Registry: 510(k)Travelpak Model Dc-202 Ref K854748
Regimes: 510(k) Registry: 510(k)Mechanical Oxygen Regulator Ref K864127
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Travomed, Inc. have in the registry?
The registry currently lists 4 devices for Travomed, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Travomed, Inc.'s devices?
Among its 4 most recently registered devices, Travomed, Inc. has devices listed in FDA 510(k) (4 devices).
What risk classes do Travomed, Inc.'s devices fall under?
Among its 4 most recently registered devices, the classes recorded for Travomed, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Travomed, Inc. in the registry?
The most recently registered devices listed for Travomed, Inc. include TRAVONEB MODEL # TONE 1, TRAVELPAK MODEL AC-102, TRAVELPAK MODEL DC-202 and MECHANICAL OXYGEN REGULATOR.