Minnesota Valley Engineering, Inc.
United StatesFDA applicant, unverified
- Devices
- 4
What Minnesota Valley Engineering, Inc. makes
Minnesota Valley Engineering, Inc. manufactures portable liquid oxygen units, including high-flow systems like the HI FLOW PORTABLE and HI FLOW 50, as well as mobility aids such as the LIBERATOR 53 and STROLLER 50. Their product line also includes the NOMAD base and portable units, designed for oxygen delivery in ambulatory settings.
These devices are classified as Class II under FDA regulations and are supported by 510(k) clearances. The company is based in the United States.
Catalogue
Hi Flow Portable Liquid Oxygen Unit Ref K875352
Regimes: 510(k) Registry: 510(k)Hi Flow 50 Ref K882328
Regimes: 510(k) Registry: 510(k)Liberator 53/Stroller 50 Ref K880101
Regimes: 510(k) Registry: 510(k)Nomad (Base Unit/Portable Unit) Ref K872449
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Minnesota Valley Engineering, Inc. have in the registry?
The registry currently lists 4 devices for Minnesota Valley Engineering, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Minnesota Valley Engineering, Inc.'s devices?
Among its 4 most recently registered devices, Minnesota Valley Engineering, Inc. has devices listed in FDA 510(k) (4 devices).
What risk classes do Minnesota Valley Engineering, Inc.'s devices fall under?
Among its 4 most recently registered devices, the classes recorded for Minnesota Valley Engineering, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Minnesota Valley Engineering, Inc. in the registry?
The most recently registered devices listed for Minnesota Valley Engineering, Inc. include HI FLOW PORTABLE LIQUID OXYGEN UNIT, HI FLOW 50, LIBERATOR 53/STROLLER 50 and NOMAD (BASE UNIT/PORTABLE UNIT).