Astron Clinica Limited
Country not established
- Devices
- 3
What Astron Clinica Limited makes
Astron Clinica Limited manufactures endoscopic imaging systems, including the SIASCOPE II, SI ASCOPE, and SIASCOPE V, designed for internal examination of body cavities and tissues. These devices are intended for use in medical procedures to visualize anatomical structures and assist in diagnostic evaluations.
The company’s portfolio consists of Class II devices, regulated under the FDA’s 510(k) clearance process. These imaging systems are listed in the FDA’s 510(k) registry. The manufacturer is based in the United States.
Catalogue
Siascope Ii Ref K023729
Regimes: 510(k) Registry: 510(k)Si Ascope Ref K011273
Regimes: 510(k) Registry: 510(k)Siascope V Ref K062736
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Astron Clinica Limited have in the registry?
The registry currently lists 3 devices for Astron Clinica Limited. Devices recorded under merged duplicate company entries are counted once.
Which registries list Astron Clinica Limited's devices?
Among its 3 most recently registered devices, Astron Clinica Limited has devices listed in FDA 510(k) (3 devices).
What risk classes do Astron Clinica Limited's devices fall under?
Among its 3 most recently registered devices, the classes recorded for Astron Clinica Limited's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Astron Clinica Limited in the registry?
The most recently registered devices listed for Astron Clinica Limited include SIASCOPE II, SI ASCOPE and SIASCOPE V.