Angiotec
Country not established
- Devices
- 2
What Angiotec makes
Angiotec manufactures the ANGIOTEC SC 1221 SCAN CONVERTER, a device designed for converting angiographic images to digital formats for diagnostic and procedural use in cardiovascular imaging.
The SC 1221 SCAN CONVERTER is classified as a Class II medical device in the US and is listed under the FDA’s 510(k) clearance pathway. The company is based in the United States.
Catalogue
Video-Dilution Tech. Mark I Instrument Ref K831057
Regimes: 510(k) Registry: 510(k)Angiotec Sc 1221 Scan Converter Ref K850330
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Angiotec have in the registry?
The registry currently lists 2 devices for Angiotec. Devices recorded under merged duplicate company entries are counted once.
Which registries list Angiotec's devices?
Among its 2 most recently registered devices, Angiotec has devices listed in FDA 510(k) (2 devices).
What risk classes do Angiotec's devices fall under?
Among its 2 most recently registered devices, the classes recorded for Angiotec's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Angiotec in the registry?
The most recently registered devices listed for Angiotec include VIDEO-DILUTION TECH. MARK I INSTRUMENT and ANGIOTEC SC 1221 SCAN CONVERTER.