Mie America, Inc.
United Statesfrom the FDA registration address FDA FEI 3000210013
- Devices
- 1
- Registrations
- FDA
- FDA recalls
- 0
At a glance
Market reach
- United States
- FDA FEI
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Mie - Gamma Camera Systems Ref K053086
Regimes: 510(k) Registry: 510(k)
Company details
- FDA FEI number
- 3000210013
- Address
- 420 BENNETT RD., ELK GROVE VILLAGE, IL, 60007
Frequently asked questions
How many devices does Mie America, Inc. have in the registry?
The registry currently lists 1 device for Mie America, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Mie America, Inc.'s devices?
Among its 1 most recently registered device, Mie America, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Mie America, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Mie America, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Mie America, Inc. in the registry?
The most recently registered devices listed for Mie America, Inc. include MIE - GAMMA CAMERA SYSTEMS.