Medical Device Manufacturer · US , Andover , MA

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

1 submissions · 1 cleared · Since 2011

Total

Cleared

Denied

Diagnos, Inc. has 1 FDA 510(k) cleared medical devices. Based in Andover, US.

Historical record: 1 cleared submissions from 2011 to 2011. Primary specialty: Ophthalmic.

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

Diagnos, 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 - Diagnos, Inc.

1 devices

1-1 of 1