Angiocor
Country not established
- Devices
- 1
What Angiocor makes
Angiocor manufactures the AngioCor Sidehole Infusion Catheter, a medical device designed for localized drug delivery during interventional procedures, particularly in coronary and peripheral vascular applications.
The device falls under FDA Class II regulation and is listed via the 510(k) clearance pathway. The manufacturer is based in the United States.
Catalogue
Angiocor Sidehole Infusion Catheter Ref K926293
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Angiocor have in the registry?
The registry currently lists 1 device for Angiocor. Devices recorded under merged duplicate company entries are counted once.
Which registries list Angiocor's devices?
Among its 1 most recently registered device, Angiocor has devices listed in FDA 510(k) (1 device).
What risk classes do Angiocor's devices fall under?
Among its 1 most recently registered device, the classes recorded for Angiocor's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Angiocor in the registry?
The most recently registered devices listed for Angiocor include ANGIOCOR SIDEHOLE INFUSION CATHETER.