American Interventional Technology
Country not established
- Devices
- 1
What American Interventional Technology makes
American Interventional Technology manufactures the PRO-GUIDE, a guidewire designed for use in coronary and peripheral vascular procedures to assist in catheter navigation and lesion crossing.
The PRO-GUIDE is classified as a Class II medical device in the US and is listed under the FDA’s 510(k) pathway. The company is based in the United States.
Catalogue
Pro-Guide Ref K911747
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does American Interventional Technology have in the registry?
The registry currently lists 1 device for American Interventional Technology. Devices recorded under merged duplicate company entries are counted once.
Which registries list American Interventional Technology's devices?
Among its 1 most recently registered device, American Interventional Technology has devices listed in FDA 510(k) (1 device).
What risk classes do American Interventional Technology's devices fall under?
Among its 1 most recently registered device, the classes recorded for American Interventional Technology's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from American Interventional Technology in the registry?
The most recently registered devices listed for American Interventional Technology include PRO-GUIDE.