Medical Device Manufacturer · US , Petaluma , CA

Acudata Software - FDA 510(k) Cleared Devices

7 submissions · 7 cleared · Since 1988

Total

Cleared

Denied

Acudata Software has 7 FDA 510(k) cleared medical devices. Based in Petaluma, US.

Historical record: 7 cleared submissions from 1988 to 1990. Primary specialty: Neurology.

Browse the FDA 510(k) cleared devices submitted by Acudata Software Filter by specialty or product code using the sidebar.

Acudata Software 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 - Acudata Software

7 devices

1-7 of 7