Medical Molding Corp. of America
United StatesFDA applicant, unverified
- Devices
- 2
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Misty Ox Laminar Diffuser Humidifier Ref K923754
Regimes: 510(k) Registry: 510(k)Misty Ox Dispos. Nebulizer Ref K841469
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Medical Molding Corp. of America have in the registry?
The registry currently lists 2 devices for Medical Molding Corp. of America. Devices recorded under merged duplicate company entries are counted once.
Which registries list Medical Molding Corp. of America's devices?
Among its 2 most recently registered devices, Medical Molding Corp. of America has devices listed in FDA 510(k) (2 devices).
What risk classes do Medical Molding Corp. of America's devices fall under?
Among its 2 most recently registered devices, the classes recorded for Medical Molding Corp. of America's devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from Medical Molding Corp. of America in the registry?
The most recently registered devices listed for Medical Molding Corp. of America include MISTY OX LAMINAR DIFFUSER HUMIDIFIER and MISTY OX DISPOS. NEBULIZER.