Aortech Critical Care, Ltd.
United KingdomFDA applicant, unverified
- Devices
- 1
What Aortech Critical Care, Ltd. makes
Aortech Critical Care, Ltd. manufactures the TRUCATH.IP, a peripheral intravenous catheter designed for critical care applications, facilitating rapid and reliable vascular access in acute medical settings.
The company’s portfolio is regulated under FDA Class II devices, with the TRUCATH.IP authorised via the 510(k) clearance pathway. The manufacturer is based in the United States.
Catalogue
Trucath.ip Ref K023368
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Aortech Critical Care, Ltd. have in the registry?
The registry currently lists 1 device for Aortech Critical Care, Ltd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Aortech Critical Care, Ltd.'s devices?
Among its 1 most recently registered device, Aortech Critical Care, Ltd. has devices listed in FDA 510(k) (1 device).
What risk classes do Aortech Critical Care, Ltd.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Aortech Critical Care, Ltd.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Aortech Critical Care, Ltd. in the registry?
The most recently registered devices listed for Aortech Critical Care, Ltd. include TRUCATH.IP.