Cyborg Corp.
Country not established
- Devices
- 1
What Cyborg Corp. makes
Cyborg Corp. manufactures pulse wave velocity monitoring devices, including the P607 model, which assesses arterial stiffness and cardiovascular health metrics.
The company’s portfolio is regulated under FDA Class II devices, with products authorised via the 510(k) clearance pathway. The manufacturer is based in the United States.
Catalogue
Monitor, Pulse Wave Velocity P607 Ref K770330
510(k) 510(k)
Frequently asked questions
How many devices does Cyborg Corp. have in the registry?
The registry currently lists 1 device for Cyborg Corp.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Cyborg Corp.'s devices?
Among its 1 most recently registered device, Cyborg Corp. has devices listed in FDA 510(k) (1 device).
What risk classes do Cyborg Corp.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Cyborg Corp.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Cyborg Corp. in the registry?
The most recently registered devices listed for Cyborg Corp. include MONITOR, PULSE WAVE VELOCITY P607.