Echo IQ, Ltd.
AustraliaFDA 510(k) applicant, unverified FDA
- Devices
- 2
- Registrations
- FDA
- FDA recalls
- 0
At a glance
Market reach
- United States
- FDA establishment
What Echo IQ, Ltd. makes
Echo IQ, Ltd. develops cardiovascular interpretive screening software designed for echocardiogram analysis, including automated measurement and assessment tools for cardiac imaging.
The company’s portfolio is regulated as Class II devices in the US, with products listed under FDA 510(k) and FDA UDI registries. The manufacturer is based in the United States.
Catalogue
- GUDID
EchoSolv AS Ref K241245
510(k) 510(k)
FDA establishments
- Echoiq Limited Sydney New South Wales · AU FEI 3033588305
Frequently asked questions
How many devices does Echo IQ, Ltd. have in the registry?
The registry currently lists 2 devices for Echo IQ, Ltd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Echo IQ, Ltd.'s devices?
Among its 2 most recently registered devices, Echo IQ, Ltd. has devices listed in FDA 510(k) (1 device) and FDA GUDID (1 device). A device can be listed in more than one registry, so these counts overlap.
What risk classes do Echo IQ, Ltd.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Echo IQ, Ltd.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Echo IQ, Ltd. in the registry?
The most recently registered devices listed for Echo IQ, Ltd. include EchoSolv AS 1.5.0 and EchoSolv AS.
Which FDA establishments are linked to Echo IQ, Ltd.?
1 FDA establishment is linked to Echo IQ, Ltd. in the registry; they are listed on the company page.