Intracath, Inc.
Country not established
- Devices
- 1
What Intracath, Inc. makes
Intracath, Inc. manufactures right atrial catheter devices, including the RAC-XXX series, designed for specific cardiac monitoring or intervention procedures.
These devices fall under FDA Class II regulation and are listed via 510(k) clearance in the United States. The company is based in the US.
Catalogue
- Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Intracath, Inc. have in the registry?
The registry currently lists 1 device for Intracath, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Intracath, Inc.'s devices?
Among its 1 most recently registered device, Intracath, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Intracath, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Intracath, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Intracath, Inc. in the registry?
The most recently registered devices listed for Intracath, Inc. include RIGHT ATRIAL CATHETER CATALOG NO. RAC - XXX SERIES.