Cortical Dynamics, Ltd.
AustraliaFDA applicant, unverified
- Devices
- 1
What Cortical Dynamics, Ltd. makes
Cortical Dynamics, Ltd. manufactures the Brain Anesthesia Response Monitor, a device designed to monitor and assess brain activity during anesthesia procedures to ensure optimal patient response.
The company’s product portfolio is regulated under Class II medical devices in the United States and is listed in the FDA’s 510(k) clearance registry. The manufacturer is based in the US.
Catalogue
Brain Anesthesia Response Monitor (Bar Monitor) Ref K213273
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Cortical Dynamics, Ltd. have in the registry?
The registry currently lists 1 device for Cortical Dynamics, Ltd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Cortical Dynamics, Ltd.'s devices?
Among its 1 most recently registered device, Cortical Dynamics, Ltd. has devices listed in FDA 510(k) (1 device).
What risk classes do Cortical Dynamics, Ltd.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Cortical Dynamics, Ltd.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Cortical Dynamics, Ltd. in the registry?
The most recently registered devices listed for Cortical Dynamics, Ltd. include Brain Anesthesia Response Monitor (Bar Monitor).