Ultramar Marketing Corp.
Country not established
- Devices
- 1
What Ultramar Marketing Corp. makes
Ultramar Marketing Corp. manufactures the NEUMOVENT 980, a mechanical ventilator designed for respiratory support in clinical settings.
The NEUMOVENT 980 is classified as a Class II medical device in the US and is listed under the FDA’s 510(k) pathway. The company is based in the United States.
Catalogue
Neumovent 980 Ref K821792
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Ultramar Marketing Corp. have in the registry?
The registry currently lists 1 device for Ultramar Marketing Corp.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Ultramar Marketing Corp.'s devices?
Among its 1 most recently registered device, Ultramar Marketing Corp. has devices listed in FDA 510(k) (1 device).
What risk classes do Ultramar Marketing Corp.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Ultramar Marketing Corp.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Ultramar Marketing Corp. in the registry?
The most recently registered devices listed for Ultramar Marketing Corp. include NEUMOVENT 980.