Digilab, Inc.
Country not established
- Devices
- 1
What Digilab, Inc. makes
Digilab, Inc. manufactures the Ocular Cerebral Vascular Monitor, a device designed to assess cerebral blood flow by analyzing ocular vasculature parameters. This tool is intended for use in clinical settings to support diagnostic or monitoring procedures related to cerebrovascular health.
The Ocular Cerebral Vascular Monitor is classified as a Class II medical device in the United States and is listed under the FDA’s 510(k) pathway. The company is based in the US.
Catalogue
Ocular Cerebral Vascular Monitor Ref K772130
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Digilab, Inc. have in the registry?
The registry currently lists 1 device for Digilab, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Digilab, Inc.'s devices?
Among its 1 most recently registered device, Digilab, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Digilab, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Digilab, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Digilab, Inc. in the registry?
The most recently registered devices listed for Digilab, Inc. include OCULAR CEREBRAL VASCULAR MONITOR.