D and D Technology, Inc.
Country not established
- Devices
- 1
What D and D Technology, Inc. makes
D and D Technology, Inc. manufactures the DIGI-FLOW, a device designed for measuring and monitoring blood flow in medical applications.
The DIGI-FLOW is classified as a Class II medical device and is listed under the FDA’s 510(k) pathway. The company is based in the United States.
Catalogue
Digi -Flow Ref K920671
510(k) 510(k)
Frequently asked questions
How many devices does D and D Technology, Inc. have in the registry?
The registry currently lists 1 device for D and D Technology, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list D and D Technology, Inc.'s devices?
Among its 1 most recently registered device, D and D Technology, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do D and D Technology, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for D and D Technology, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from D and D Technology, Inc. in the registry?
The most recently registered devices listed for D and D Technology, Inc. include DIGI -FLOW.