Angi-Pak Corp.
United StatesFDA applicant, unverified
- Devices
- 2
What Angi-Pak Corp. makes
Angi-Pak Corp. makes medical devices such as the CORDIPAK ANGIOGRAPHY TRAY and CORDIPAK CARDIAC CATHETERIZATION PACK, which are used in angiography and cardiac catheterization procedures.
The company's portfolio is regulated as Class II devices and is listed in the FDA 510(k) registry, with the company based in the US.
Catalogue
Cordipak Angiography Tray Ref K863336
Regimes: 510(k) Registry: 510(k)Cordipak Cardiac Catheterization Pack Ref K863337
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Angi-Pak Corp. have in the registry?
The registry currently lists 2 devices for Angi-Pak Corp.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Angi-Pak Corp.'s devices?
Among its 2 most recently registered devices, Angi-Pak Corp. has devices listed in FDA 510(k) (2 devices).
What risk classes do Angi-Pak Corp.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Angi-Pak Corp.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Angi-Pak Corp. in the registry?
The most recently registered devices listed for Angi-Pak Corp. include CORDIPAK ANGIOGRAPHY TRAY and CORDIPAK CARDIAC CATHETERIZATION PACK.