Cardio-Pak
Country not established
- Devices
- 1
What Cardio-Pak makes
Cardio-Pak specializes in custom angiography packs designed for use in cardiac imaging procedures, providing sterile and pre-assembled trays of supplies required for coronary angiography.
These products are regulated as Class II medical devices under the FDA’s 510(k) pathway and are listed in the U.S. regulatory database. The company operates from the United States.
Catalogue
Cardio-Pak Angiography Custom Packs Ref K902475
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Cardio-Pak have in the registry?
The registry currently lists 1 device for Cardio-Pak. Devices recorded under merged duplicate company entries are counted once.
Which registries list Cardio-Pak's devices?
Among its 1 most recently registered device, Cardio-Pak has devices listed in FDA 510(k) (1 device).
What risk classes do Cardio-Pak's devices fall under?
Among its 1 most recently registered device, the classes recorded for Cardio-Pak's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Cardio-Pak in the registry?
The most recently registered devices listed for Cardio-Pak include CARDIO-PAK ANGIOGRAPHY CUSTOM PACKS.