Activiews, Ltd.
Country not established
- Devices
- 3
What Activiews, Ltd. makes
Activiews, Ltd. manufactures CT-Guide Needle Guidance Systems designed to assist in precise needle placement during computed tomography (CT)-guided procedures. These systems integrate with CT imaging to enhance accuracy and reduce procedural risks for interventions such as biopsies or drainages.
The company’s needle guidance systems are classified as Class II devices under FDA regulations and are authorised through the 510(k) clearance process. The portfolio is listed in the FDA’s 510(k) registry, reflecting compliance with U.S. medical device requirements.
Catalogue
Ct-Guide Needle Guidance System Ref K120300
Regimes: 510(k) Registry: 510(k)Ct-Guide Needle Guidance System Ref K110812
Regimes: 510(k) Registry: 510(k)Ct-Guide Needle Guidance System Ref K113063
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Activiews, Ltd. have in the registry?
The registry currently lists 3 devices for Activiews, Ltd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Activiews, Ltd.'s devices?
Among its 3 most recently registered devices, Activiews, Ltd. has devices listed in FDA 510(k) (3 devices).
What risk classes do Activiews, Ltd.'s devices fall under?
Among its 3 most recently registered devices, the classes recorded for Activiews, Ltd.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Activiews, Ltd. in the registry?
The most recently registered devices listed for Activiews, Ltd. include CT-GUIDE NEEDLE GUIDANCE SYSTEM.