Maxi-Aids, Inc.
United StatesFDA applicant, unverified
- Devices
- 2
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
- Regimes: 510(k) Registry: 510(k)
Hf Mega Ear Ref K960567
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Maxi-Aids, Inc. have in the registry?
The registry currently lists 2 devices for Maxi-Aids, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Maxi-Aids, Inc.'s devices?
Among its 2 most recently registered devices, Maxi-Aids, Inc. has devices listed in FDA 510(k) (2 devices).
What risk classes do Maxi-Aids, Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Maxi-Aids, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Maxi-Aids, Inc. in the registry?
The most recently registered devices listed for Maxi-Aids, Inc. include REIZEN TALKING BLOOD PRESSURE MONITOR, MODEL #SF860T and HF MEGA EAR.