D/P, Inc.
Country not established
- Devices
- 1
Catalogue
Vein Graft Cannula Ref K791832
510(k) 510(k)
Frequently asked questions
How many devices does D/P, Inc. have in the registry?
The registry currently lists 1 device for D/P, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list D/P, Inc.'s devices?
Among its 1 most recently registered device, D/P, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do D/P, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for D/P, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from D/P, Inc. in the registry?
The most recently registered devices listed for D/P, Inc. include VEIN GRAFT CANNULA.