Multiscan, Inc.
Country not established
- Devices
- 1
What Multiscan, Inc. makes
Multiscan, Inc. makes the MULTISCAN 7 device.
The MULTISCAN 7 is a Class II medical device listed in the FDA 510(k) registry, and the company is based in the United States.
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Multiscan 7 Ref K853852
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Multiscan, Inc. have in the registry?
The registry currently lists 1 device for Multiscan, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Multiscan, Inc.'s devices?
Among its 1 most recently registered device, Multiscan, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Multiscan, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Multiscan, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Multiscan, Inc. in the registry?
The most recently registered devices listed for Multiscan, Inc. include MULTISCAN 7.