Vitacon Medical, Inc.
CanadaFDA applicant, unverified
- Devices
- 1
What Vitacon Medical, Inc. makes
Vitacon Medical, Inc. manufactures the VITASCAN LT SCANMASTER, which is a Class II medical device.
The company is based in the US and its devices are listed in the FDA 510(k) registry.
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Vitascan Lt Scanmaster Ref K121689
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Vitacon Medical, Inc. have in the registry?
The registry currently lists 1 device for Vitacon Medical, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Vitacon Medical, Inc.'s devices?
Among its 1 most recently registered device, Vitacon Medical, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Vitacon Medical, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Vitacon Medical, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Vitacon Medical, Inc. in the registry?
The most recently registered devices listed for Vitacon Medical, Inc. include VITASCAN LT SCANMASTER.