Iagnon Corp.
Country not established
- Devices
- 1
What Iagnon Corp. makes
Iagnon Corp. manufactures the DIAGNON Ferritin 125I RIA Kit, a diagnostic test designed to measure ferritin levels in blood samples using radioimmunoassay (RIA) technology.
The company’s diagnostic products are classified as Class II devices under FDA regulations and are listed via the 510(k) pathway. The portfolio is authorised for use in the United States.
Catalogue
Diagnon Ferritin 125 I Ria Kit Ref K830580
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Iagnon Corp. have in the registry?
The registry currently lists 1 device for Iagnon Corp.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Iagnon Corp.'s devices?
Among its 1 most recently registered device, Iagnon Corp. has devices listed in FDA 510(k) (1 device).
What risk classes do Iagnon Corp.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Iagnon Corp.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Iagnon Corp. in the registry?
The most recently registered devices listed for Iagnon Corp. include DIAGNON FERRITIN 125 I RIA KIT.