Chiron Corp.
United StatesFDA applicant, unverified
- Devices
- 2
What Chiron Corp. makes
Chiron Corp. manufactures automated chemiluminescence systems, including the ACS:180 BR system designed for the quantitation of cancer antigen 27.29.
The company is based in the US, and its portfolio consists of Class II medical devices that are listed in the FDA 510(k) regulatory registry.
Catalogue
ACS:180 Br (Automated Chemiluminescence System For The Quantitation Of Cancer Antigen 27.29) Ref K981698
Regimes: 510(k) Registry: 510(k)Acs 180 Br (Automated Chemiluminescence System) Ref K980190
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Chiron Corp. have in the registry?
The registry currently lists 2 devices for Chiron Corp.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Chiron Corp.'s devices?
Among its 2 most recently registered devices, Chiron Corp. has devices listed in FDA 510(k) (2 devices).
What risk classes do Chiron Corp.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Chiron Corp.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Chiron Corp. in the registry?
The most recently registered devices listed for Chiron Corp. include ACS:180 BR (AUTOMATED CHEMILUMINESCENCE SYSTEM FOR THE QUANTITATION OF CANCER ANTIGEN 27.29) and ACS 180 BR (AUTOMATED CHEMILUMINESCENCE SYSTEM).