Huntleigh Diagnostics, Ltd.
Country not established
- Devices
- 3
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Fetal Assist Ref K002548
Regimes: 510(k) Registry: 510(k)Baby Dopplex 4000 (BD4000) Ref K001677
Regimes: 510(k) Registry: 510(k)Modification To Fetal Assist Ref K020390
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Huntleigh Diagnostics, Ltd. have in the registry?
The registry currently lists 3 devices for Huntleigh Diagnostics, Ltd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Huntleigh Diagnostics, Ltd.'s devices?
Among its 3 most recently registered devices, Huntleigh Diagnostics, Ltd. has devices listed in FDA 510(k) (3 devices).
What risk classes do Huntleigh Diagnostics, Ltd.'s devices fall under?
Among its 3 most recently registered devices, the classes recorded for Huntleigh Diagnostics, Ltd.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Huntleigh Diagnostics, Ltd. in the registry?
The most recently registered devices listed for Huntleigh Diagnostics, Ltd. include FETAL ASSIST, BABY DOPPLEX 4000 (BD4000) and MODIFICATION TO FETAL ASSIST.