Acculab
Country not established
- Devices
- 1
What Acculab makes
Acculab manufactures automatic biochemical analyzers designed for clinical chemistry testing, enabling automated processing of blood and serum samples to measure key biochemical parameters.
The company’s products are regulated as Class I devices under FDA 510(k) clearance requirements and are listed in the FDA’s 510(k) database. The manufacturer is based in the United States.
Catalogue
Automatic Biochemical Analyzer Ref K810063
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Acculab have in the registry?
The registry currently lists 1 device for Acculab. Devices recorded under merged duplicate company entries are counted once.
Which registries list Acculab's devices?
Among its 1 most recently registered device, Acculab has devices listed in FDA 510(k) (1 device).
What risk classes do Acculab's devices fall under?
Among its 1 most recently registered device, the classes recorded for Acculab's devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Acculab in the registry?
The most recently registered devices listed for Acculab include AUTOMATIC BIOCHEMICAL ANALYZER.