Medical Device Manufacturer · US , Palo Alto , CA

Cbyon, Inc. - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 2000

Total

Cleared

Denied

Cbyon, Inc. has 2 FDA 510(k) cleared medical devices. Based in Palo Alto, US.

Historical record: 2 cleared submissions from 2000 to 2001. Primary specialty: Neurology.

Browse the FDA 510(k) cleared devices submitted by Cbyon, Inc. Filter by specialty or product code using the sidebar.

Cbyon, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Cbyon, Inc.

2 devices

1-2 of 2