Ocg Technology, Inc.
United StatesFDA applicant, unverified
- Devices
- 3
What Ocg Technology, Inc. makes
Ocg Technology, Inc. manufactures devices for cardiac signal analysis, including cardiointegram/cardiointegraph systems and their modified versions. Their portfolio includes the Expert Models RTS 2000 and RTS 2000H, which are designed for assessing cardiac electrical activity and related metrics.
These devices are classified as Class II under FDA regulations and are supported by 510(k) clearance records. The company is based in the United States.
Catalogue
Modification Of Cardiointegram/Cardiointegraph Ref K863153
Regimes: 510(k) Registry: 510(k)Cardiointegram Ref K812971
Regimes: 510(k) Registry: 510(k)The Expert Models Rts 2000 And Rts 2000H Ref K862947
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Ocg Technology, Inc. have in the registry?
The registry currently lists 3 devices for Ocg Technology, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Ocg Technology, Inc.'s devices?
Among its 3 most recently registered devices, Ocg Technology, Inc. has devices listed in FDA 510(k) (3 devices).
What risk classes do Ocg Technology, Inc.'s devices fall under?
Among its 3 most recently registered devices, the classes recorded for Ocg Technology, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Ocg Technology, Inc. in the registry?
The most recently registered devices listed for Ocg Technology, Inc. include MODIFICATION OF CARDIOINTEGRAM/CARDIOINTEGRAPH, CARDIOINTEGRAM and THE EXPERT MODELS RTS 2000 AND RTS 2000H.