Merge Technologies, Inc.
Country not established
- Devices
- 1
What Merge Technologies, Inc. makes
Merge Technologies, Inc. manufactures the MVP, a multi-vendor protocol converter designed to facilitate communication between different medical device systems.
The MVP is classified as a Class I device under FDA regulations and is listed in the FDA’s 510(k) registry. The company is based in the United States.
Catalogue
Mvp (Multi-Vendor Protocol Convertor) Ref K900227
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Merge Technologies, Inc. have in the registry?
The registry currently lists 1 device for Merge Technologies, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Merge Technologies, Inc.'s devices?
Among its 1 most recently registered device, Merge Technologies, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Merge Technologies, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Merge Technologies, Inc.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Merge Technologies, Inc. in the registry?
The most recently registered devices listed for Merge Technologies, Inc. include MVP (MULTI-VENDOR PROTOCOL CONVERTOR).