Biocentrex
Country not established
- Devices
- 1
What Biocentrex makes
Biocentrex manufactures the Biocentrex Cardiac Panel, a diagnostic in vitro device used for cardiac biomarker testing to aid in the evaluation of acute coronary syndromes and other cardiac conditions.
The device is classified as Class II under FDA regulations and is authorised via 510(k) clearance. The company is based in the United States.
Catalogue
Biocentrex Cardiac Panel Ref K033155
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Biocentrex have in the registry?
The registry currently lists 1 device for Biocentrex. Devices recorded under merged duplicate company entries are counted once.
Which registries list Biocentrex's devices?
Among its 1 most recently registered device, Biocentrex has devices listed in FDA 510(k) (1 device).
What risk classes do Biocentrex's devices fall under?
Among its 1 most recently registered device, the classes recorded for Biocentrex's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Biocentrex in the registry?
The most recently registered devices listed for Biocentrex include BIOCENTREX CARDIAC PANEL.