Cybernetic Medical, Inc.
United StatesFDA 510(k) applicant, unverified
- Devices
- 2
What Cybernetic Medical, Inc. makes
Cybernetic Medical, Inc. manufactures a heart rate monitor and a relaxation course model designed for therapeutic use. The heart rate monitor is intended for continuous cardiac monitoring, while the relaxation course model appears to be a device for guided stress reduction or biofeedback sessions.
The company’s portfolio is regulated under Class II devices in the US, with products authorised through the FDA’s 510(k) clearance process. These devices are listed in the FDA’s 510(k) registry, and the manufacturer is based in the United States.
Catalogue
Monitor, Heart Rate Ref K781166
510(k) 510(k)Relaxation Course Model 1000 Ref K770787
510(k) 510(k)
Frequently asked questions
How many devices does Cybernetic Medical, Inc. have in the registry?
The registry currently lists 2 devices for Cybernetic Medical, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Cybernetic Medical, Inc.'s devices?
Among its 2 most recently registered devices, Cybernetic Medical, Inc. has devices listed in FDA 510(k) (2 devices).
What risk classes do Cybernetic Medical, Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Cybernetic Medical, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Cybernetic Medical, Inc. in the registry?
The most recently registered devices listed for Cybernetic Medical, Inc. include MONITOR, HEART RATE and RELAXATION COURSE MODEL 1000.