Medatron, Inc.
Country not established
- Devices
- 1
What Medatron, Inc. makes
Medatron, Inc. manufactures cuvette discs, which are disposable sample holders used in laboratory analyzers for blood chemistry and clinical diagnostics. These devices facilitate automated testing by holding liquid samples for optical measurement during assays.
The cuvette discs fall under Class I regulatory classification in the U.S. and are listed via 510(k) clearance with the FDA. The company is headquartered in the United States.
Catalogue
Medatron Cuvette Disc Ref K873656
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Medatron, Inc. have in the registry?
The registry currently lists 1 device for Medatron, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Medatron, Inc.'s devices?
Among its 1 most recently registered device, Medatron, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Medatron, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Medatron, Inc.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Medatron, Inc. in the registry?
The most recently registered devices listed for Medatron, Inc. include MEDATRON CUVETTE DISC.