Graftcath, Inc.
Country not established
- Devices
- 1
What Graftcath, Inc. makes
Graftcath, Inc. manufactures the HERO Vascular Access Device, a medical implant designed for vascular access in patients requiring hemodialysis or other long-term intravenous therapies.
The HERO Vascular Access Device 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
Hero Vascular Access Device Ref K071778
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Graftcath, Inc. have in the registry?
The registry currently lists 1 device for Graftcath, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Graftcath, Inc.'s devices?
Among its 1 most recently registered device, Graftcath, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Graftcath, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Graftcath, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Graftcath, Inc. in the registry?
The most recently registered devices listed for Graftcath, Inc. include HERO VASCULAR ACCESS DEVICE.