Cardiarc, Ltd.
Country not established
- Devices
- 1
What Cardiarc, Ltd. makes
Cardiarc, Ltd. manufactures the Cardiarc SPECT Imaging Device (Model CQ103-RV2), a single-photon emission computed tomography (SPECT) system designed for cardiac imaging to assess myocardial perfusion and function.
The company’s portfolio is regulated under FDA’s Class II device classification and is listed in the 510(k) premarket notification process. The manufacturer is based in the United States.
Catalogue
Cardiarc Spect Imaging Device, Model CQ103-RV2 Ref K053062
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Cardiarc, Ltd. have in the registry?
The registry currently lists 1 device for Cardiarc, Ltd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Cardiarc, Ltd.'s devices?
Among its 1 most recently registered device, Cardiarc, Ltd. has devices listed in FDA 510(k) (1 device).
What risk classes do Cardiarc, Ltd.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Cardiarc, Ltd.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Cardiarc, Ltd. in the registry?
The most recently registered devices listed for Cardiarc, Ltd. include CARDIARC SPECT IMAGING DEVICE, MODEL CQ103-RV2.