Bisico GmbH & CO KG is one of 68 FDA 510(k) medical device manufacturers from Netherlands in the dataset, ranked by real submission volume.
Bisico GmbH & CO KG - FDA 510(k) Cleared Devices
1
Total
1
Cleared
0
Denied
Bisico GmbH & CO KG has 1 FDA 510(k) cleared medical devices. Based in Amsterdam, NL.
Historical record: 1 cleared submissions from 2007 to 2007. Primary specialty: Dental.
Browse the FDA 510(k) cleared devices submitted by Bisico GmbH & CO KG Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Bisico GmbH & CO KG
1 devices