Cetus Corp.
United StatesFDA applicant, unverified
- Devices
- 3
What Cetus Corp. makes
Cetus Corp. manufactures automated liquid handling systems, including the PROGROUP™ system for precise fluid processing in laboratory settings. The company also produces diagnostic reagents like the EPICHROME PAP, a test for detecting protein in urine, and the CETUS CMV IHA, an immunoassay for cytomegalovirus antibodies.
These devices are regulated under FDA’s 510(k) pathway, with classifications ranging from Class I to Class II. The company’s products are listed in the FDA’s 510(k) database, and Cetus Corp. is headquartered in the United States.
Catalogue
Progroup (Tm) Automated Liquid Handling System Ref K861580
Regimes: 510(k) Registry: 510(k)Epichrome Pap Ref K844968
Regimes: 510(k) Registry: 510(k)Cetus Cmv Iha Ref K822965
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Cetus Corp. have in the registry?
The registry currently lists 3 devices for Cetus Corp.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Cetus Corp.'s devices?
Among its 3 most recently registered devices, Cetus Corp. has devices listed in FDA 510(k) (3 devices).
What risk classes do Cetus Corp.'s devices fall under?
Among its 3 most recently registered devices, the classes recorded for Cetus Corp.'s devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from Cetus Corp. in the registry?
The most recently registered devices listed for Cetus Corp. include PROGROUP (TM) AUTOMATED LIQUID HANDLING SYSTEM, EPICHROME PAP and CETUS CMV IHA.