Revolutionary Medical Devices, Inc.
United StatesFDA applicant, unverified
- Devices
- 2
What Revolutionary Medical Devices, Inc. makes
Revolutionary Medical Devices, Inc. manufactures the SuperNO2VA Device and the SuperNO2VA Et Device. These products function as respiratory and airway management devices.
The company is based in the United States, and its portfolio includes Class I and Class II medical devices. These products are listed in the FDA 510(k) regulatory registry.
Catalogue
SuperNO2VA Device Ref K163277
Regimes: 510(k) Registry: 510(k)SuperNO2VA Et Device Ref K173147
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Revolutionary Medical Devices, Inc. have in the registry?
The registry currently lists 2 devices for Revolutionary Medical Devices, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Revolutionary Medical Devices, Inc.'s devices?
Among its 2 most recently registered devices, Revolutionary Medical Devices, Inc. has devices listed in FDA 510(k) (2 devices).
What risk classes do Revolutionary Medical Devices, Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Revolutionary Medical Devices, Inc.'s devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from Revolutionary Medical Devices, Inc. in the registry?
The most recently registered devices listed for Revolutionary Medical Devices, Inc. include SuperNO2VA Device and SuperNO2VA Et Device.