Medtron Development, Ltd.
Country not established
- Devices
- 1
What Medtron Development, Ltd. makes
Medtron Development, Ltd. manufactures the ENDOPUMP, a medical device designed for controlled fluid delivery in endoscopic procedures.
The ENDOPUMP is classified as a Class II device under FDA regulations and is listed via the 510(k) pathway. The company is based in the United States.
Catalogue
Endopump Ref K811783
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Medtron Development, Ltd. have in the registry?
The registry currently lists 1 device for Medtron Development, Ltd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Medtron Development, Ltd.'s devices?
Among its 1 most recently registered device, Medtron Development, Ltd. has devices listed in FDA 510(k) (1 device).
What risk classes do Medtron Development, Ltd.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Medtron Development, Ltd.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Medtron Development, Ltd. in the registry?
The most recently registered devices listed for Medtron Development, Ltd. include ENDOPUMP.