Aranco Diagnostic Laboratories, Inc.
Country not established
- Devices
- 1
What Aranco Diagnostic Laboratories, Inc. makes
Aranco Diagnostic Laboratories, Inc. manufactures ARANTROL, a diagnostic reagent or test system designed for in vitro clinical analysis, likely used in laboratory settings for specific medical evaluations.
The company’s portfolio is regulated under FDA’s Class II device classification and requires 510(k) clearance. ARANTROL is listed in the FDA’s 510(k) registry. The manufacturer is based in the United States.
Catalogue
Arantrol Ref K780835
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Aranco Diagnostic Laboratories, Inc. have in the registry?
The registry currently lists 1 device for Aranco Diagnostic Laboratories, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Aranco Diagnostic Laboratories, Inc.'s devices?
Among its 1 most recently registered device, Aranco Diagnostic Laboratories, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Aranco Diagnostic Laboratories, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Aranco Diagnostic Laboratories, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Aranco Diagnostic Laboratories, Inc. in the registry?
The most recently registered devices listed for Aranco Diagnostic Laboratories, Inc. include ARANTROL.