Bioscreen, Inc.
Country not established
- Devices
- 1
What Bioscreen, Inc. makes
Bioscreen, Inc. manufactures QC-BEADS, a diagnostic device used for quality control in laboratory testing, ensuring accuracy and reliability of assay results.
The QC-BEADS portfolio is regulated as Class II medical devices in the US and is listed under the FDA’s 510(k) clearance process. The company is based in the United States.
Catalogue
Qc-Beads Ref K042750
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Bioscreen, Inc. have in the registry?
The registry currently lists 1 device for Bioscreen, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Bioscreen, Inc.'s devices?
Among its 1 most recently registered device, Bioscreen, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Bioscreen, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Bioscreen, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Bioscreen, Inc. in the registry?
The most recently registered devices listed for Bioscreen, Inc. include QC-BEADS.