Medphone Corp.
United StatesFDA applicant, unverified
- Devices
- 2
What Medphone Corp. makes
Medphone Corp. makes defibrillator systems, including the MDPHONE CELLULAR + RESCUE defibrillator system and the telephone defibrillator system.
These devices are classified as Class II medical devices and are listed in the FDA 510(k) registry. The company is based in the United States.
Catalogue
Mdphone Cellular + Rescue (Defib System) Ref K911604
Regimes: 510(k) Registry: 510(k)Telephone Defibrillator System Ref K864257
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Medphone Corp. have in the registry?
The registry currently lists 2 devices for Medphone Corp.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Medphone Corp.'s devices?
Among its 2 most recently registered devices, Medphone Corp. has devices listed in FDA 510(k) (2 devices).
What risk classes do Medphone Corp.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Medphone Corp.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Medphone Corp. in the registry?
The most recently registered devices listed for Medphone Corp. include MDPHONE CELLULAR + RESCUE (DEFIB SYSTEM) and TELEPHONE DEFIBRILLATOR SYSTEM.