Hemodiagnostica, LLC
Country not established
- Devices
- 1
What Hemodiagnostica, LLC makes
Hemodiagnostica, LLC manufactures clinical chemistry systems, including the SDI CA480 and SATURNO 300, designed for laboratory analysis of blood and other biological samples to measure biochemical parameters.
These systems are regulated as Class II devices under FDA 510(k) clearance requirements and are listed in the FDA’s 510(k) database. The company is based in the United States.
Catalogue
- Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Hemodiagnostica, LLC have in the registry?
The registry currently lists 1 device for Hemodiagnostica, LLC. Devices recorded under merged duplicate company entries are counted once.
Which registries list Hemodiagnostica, LLC's devices?
Among its 1 most recently registered device, Hemodiagnostica, LLC has devices listed in FDA 510(k) (1 device).
What risk classes do Hemodiagnostica, LLC's devices fall under?
Among its 1 most recently registered device, the classes recorded for Hemodiagnostica, LLC's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Hemodiagnostica, LLC in the registry?
The most recently registered devices listed for Hemodiagnostica, LLC include SDI CA480 CLINICAL CHEMISTRY SYSTEM; SATURNO 300 CLINICAL CHEMISTRY SYSTEM.