Actio, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Actio, Inc. - FDA 510(k) Cleared Devices
4
Total
4
Cleared
0
Denied
Actio, Inc. has 4 FDA 510(k) cleared medical devices. Based in Oakland, US.
Historical record: 4 cleared submissions from 1989 to 1990. Primary specialty: Chemistry.
Browse the FDA 510(k) cleared devices submitted by Actio, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Actio, Inc.
4 devices