Dana Laboratories
Country not established
- Devices
- 2
What Dana Laboratories makes
Dana Laboratories manufactures hemodialysis concentrate and hemodialysis concentrate additives, which are used in the preparation of dialysis solutions for patients undergoing hemodialysis treatment.
These products are classified as Class II medical devices under FDA regulations and are listed via the 510(k) pathway. The company is based in the United States.
Catalogue
Hemodialysis Concentrate Ref K854391
Regimes: 510(k) Registry: 510(k)Hemodialysis Concentrate Additives Ref K851431
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Dana Laboratories have in the registry?
The registry currently lists 2 devices for Dana Laboratories. Devices recorded under merged duplicate company entries are counted once.
Which registries list Dana Laboratories's devices?
Among its 2 most recently registered devices, Dana Laboratories has devices listed in FDA 510(k) (2 devices).
What risk classes do Dana Laboratories's devices fall under?
Among its 2 most recently registered devices, the classes recorded for Dana Laboratories's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Dana Laboratories in the registry?
The most recently registered devices listed for Dana Laboratories include HEMODIALYSIS CONCENTRATE and HEMODIALYSIS CONCENTRATE ADDITIVES.