Mdi Instruments, Inc.
United StatesFDA applicant, unverified
- Devices
- 2
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Earcheck Ref K971859
Regimes: 510(k) Registry: 510(k)Earcheck Pro Ref K970685
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Mdi Instruments, Inc. have in the registry?
The registry currently lists 2 devices for Mdi Instruments, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Mdi Instruments, Inc.'s devices?
Among its 2 most recently registered devices, Mdi Instruments, Inc. has devices listed in FDA 510(k) (2 devices).
What risk classes do Mdi Instruments, Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Mdi Instruments, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Mdi Instruments, Inc. in the registry?
The most recently registered devices listed for Mdi Instruments, Inc. include EARCHECK and EARCHECK PRO.