Irex Corp.
United StatesFDA applicant, unverified
- Devices
- 10
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Irex 730 Mechanical Sector Scanner Ref K842408
Regimes: 510(k) Registry: 510(k)Irex System Ii 2D/Doppler Imaging System Ref K827370
Regimes: 510(k) Registry: 510(k)Doppler Ultrasound Blood Flowmeter Ref K811246
Regimes: 510(k) Registry: 510(k)Color Doppler 880 Ref K843643
Regimes: 510(k) Registry: 510(k)Irex Ps, Portable Scanner And 118 Ref K844404
Regimes: 510(k) Registry: 510(k)Irex Real Time Phased Array System Ref K791317
Regimes: 510(k) Registry: 510(k)Irex 2D/Doppler Phase Array Imaging Sys. Ref K813544
Regimes: 510(k) Registry: 510(k)System Ii Ref K771372
Regimes: 510(k) Registry: 510(k)Irex 720 Sector Scanner Ref K840139
Regimes: 510(k) Registry: 510(k)Irex Cardioplan Ref K792525
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Irex Corp. have in the registry?
The registry currently lists 10 devices for Irex Corp.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Irex Corp.'s devices?
Among its 10 most recently registered devices, Irex Corp. has devices listed in FDA 510(k) (10 devices).
What risk classes do Irex Corp.'s devices fall under?
Among its 10 most recently registered devices, the classes recorded for Irex Corp.'s devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from Irex Corp. in the registry?
The most recently registered devices listed for Irex Corp. include IREX 730 MECHANICAL SECTOR SCANNER, IREX SYSTEM II 2D/DOPPLER IMAGING SYSTEM, DOPPLER ULTRASOUND BLOOD FLOWMETER and COLOR DOPPLER 880.