Medical Devices/Padpro, Inc.
Country not established
- Devices
- 1
What Medical Devices/Padpro, Inc. makes
The company produces the DT2200, a defibrillator cable tester designed to verify the functionality and integrity of defibrillator cables before use in medical procedures.
The DT2200 is classified as a Class II medical device and is listed under FDA’s 510(k) pathway. The manufacturer is based in the United States.
Catalogue
Defibrillator Cable Tester, Model DT2200 Ref K061606
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Medical Devices/Padpro, Inc. have in the registry?
The registry currently lists 1 device for Medical Devices/Padpro, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Medical Devices/Padpro, Inc.'s devices?
Among its 1 most recently registered device, Medical Devices/Padpro, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Medical Devices/Padpro, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Medical Devices/Padpro, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Medical Devices/Padpro, Inc. in the registry?
The most recently registered devices listed for Medical Devices/Padpro, Inc. include DEFIBRILLATOR CABLE TESTER, MODEL DT2200.