Vital Canada, Inc.
CanadaFDA applicant, unverified
- Devices
- 1
What Vital Canada, Inc. makes
Vital Canada, Inc. manufactures the VI-FLOW PUMP WITH VI-SET, a device designed for controlled fluid delivery in medical applications.
The VI-FLOW PUMP WITH VI-SET is classified as a Class II medical device and is listed under the FDA’s 510(k) pathway. The company is based in the United States.
Catalogue
Vi-Flow Pump With Vi-Set Ref K851821
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Vital Canada, Inc. have in the registry?
The registry currently lists 1 device for Vital Canada, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Vital Canada, Inc.'s devices?
Among its 1 most recently registered device, Vital Canada, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Vital Canada, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Vital Canada, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Vital Canada, Inc. in the registry?
The most recently registered devices listed for Vital Canada, Inc. include VI-FLOW PUMP WITH VI-SET.