Actus, Inc.
United StatesFDA applicant, unverified
- Devices
- 4
What Actus, Inc. makes
Actus, Inc. manufactures automated well type gamma counters and digital radiation detectors, designed for measuring gamma radiation in laboratory settings. These devices are used to quantify radioactivity in samples, supporting applications in environmental monitoring, nuclear medicine, and research.
The company’s products are classified as Class I medical devices under FDA regulations and are listed in the 510(k) clearance registry. Actus, Inc. is based in the United States.
Catalogue
Auto. Well Type Gamma Counters Ref K771614
Regimes: 510(k) Registry: 510(k)Digital Radiation Detector Ref K771301
Regimes: 510(k) Registry: 510(k)Well Type Gamma Counter Ref K771613
Regimes: 510(k) Registry: 510(k)Well Type Gamma Counter Ref K771612
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Actus, Inc. have in the registry?
The registry currently lists 4 devices for Actus, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Actus, Inc.'s devices?
Among its 4 most recently registered devices, Actus, Inc. has devices listed in FDA 510(k) (4 devices).
What risk classes do Actus, Inc.'s devices fall under?
Among its 4 most recently registered devices, the classes recorded for Actus, Inc.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Actus, Inc. in the registry?
The most recently registered devices listed for Actus, Inc. include AUTO. WELL TYPE GAMMA COUNTERS, DIGITAL RADIATION DETECTOR and WELL TYPE GAMMA COUNTER.