Caradyne, Ltd.
Country not established
- Devices
- 5
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Criterion 60 Or Pm 60 Ref K000959
Regimes: 510(k) Registry: 510(k)Criterion 40 Or Pm 40 Ref K992101
Regimes: 510(k) Registry: 510(k)- Regimes: 510(k) Registry: 510(k)
Guardian Neonate Cpap/Humidification System Ref K040862
Regimes: 510(k) Registry: 510(k)Oxicheck Ref K023565
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Caradyne, Ltd. have in the registry?
The registry currently lists 5 devices for Caradyne, Ltd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Caradyne, Ltd.'s devices?
Among its 5 most recently registered devices, Caradyne, Ltd. has devices listed in FDA 510(k) (5 devices).
What risk classes do Caradyne, Ltd.'s devices fall under?
Among its 5 most recently registered devices, the classes recorded for Caradyne, Ltd.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Caradyne, Ltd. in the registry?
The most recently registered devices listed for Caradyne, Ltd. include CRITERION 60 OR PM 60, CRITERION 40 OR PM 40, WHISPERFLOW OXYGEN FLOW GENERATOR - ADJUSTABLE MODEL WF 8500 WHISPERFLOW OXYGEN FLOW GENERATOR - FIXED MODEL WF 8530 WH and GUARDIAN NEONATE CPAP/HUMIDIFICATION SYSTEM.