Veritract, Inc.
Country not established
- Devices
- 1
What Veritract, Inc. makes
Veritract, Inc. manufactures the Veritract Enteral Feeding Tube System, a medical device designed for enteral nutrition delivery.
The company’s portfolio is regulated under FDA Class II devices and is listed via the 510(k) clearance process. The manufacturer is based in the United States.
Catalogue
Veritract Enteral Feeding Tube System Ref K133334
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Veritract, Inc. have in the registry?
The registry currently lists 1 device for Veritract, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Veritract, Inc.'s devices?
Among its 1 most recently registered device, Veritract, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Veritract, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Veritract, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Veritract, Inc. in the registry?
The most recently registered devices listed for Veritract, Inc. include VERITRACT ENTERAL FEEDING TUBE SYSTEM.