Ambu Innovation GmbH is one of 234 FDA 510(k) medical device manufacturers from Germany in the dataset, ranked by real submission volume.
Ambu Innovation GmbH - FDA 510(k) Cleared Devices
Recent clearances: Ambu Duodeno System
1
Total
1
Cleared
0
Denied
Ambu Innovation GmbH has 1 FDA 510(k) cleared medical devices. Based in Kissing, DE.
Historical record: 1 cleared submissions from 2020 to 2020. Primary specialty: Gastroenterology & Urology.
Browse the FDA 510(k) cleared devices submitted by Ambu Innovation GmbH Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Ambu, Inc. as regulatory consultant.
FDA 510(k) Regulatory Record - Ambu Innovation GmbH
1 devices