Travis Industries, Inc.
United StatesFDA applicant, unverified
- Devices
- 3
What Travis Industries, Inc. makes
Travis Industries, Inc. manufactures professional medical monitors, including models designed to prevent water damage, such as the Wet-No-More Monitor. These devices are intended for clinical use in healthcare settings to display patient vitals and other diagnostic data.
The company’s products are classified as Class II devices under FDA regulations and are authorised through the 510(k) clearance process. These devices are listed in the FDA’s 510(k) registry, and the manufacturer is based in the United States.
Catalogue
Professional Monitor Ref K901907
Regimes: 510(k) Registry: 510(k)Wet-No-More Monitor Ref K901906
Regimes: 510(k) Registry: 510(k)Wet-No-More Monitor Ref K903856
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Travis Industries, Inc. have in the registry?
The registry currently lists 3 devices for Travis Industries, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Travis Industries, Inc.'s devices?
Among its 3 most recently registered devices, Travis Industries, Inc. has devices listed in FDA 510(k) (3 devices).
What risk classes do Travis Industries, Inc.'s devices fall under?
Among its 3 most recently registered devices, the classes recorded for Travis Industries, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Travis Industries, Inc. in the registry?
The most recently registered devices listed for Travis Industries, Inc. include PROFESSIONAL MONITOR and WET-NO-MORE MONITOR.