Kaweco GmbH is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Kaweco GmbH - FDA 510(k) Cleared Devices
1
Total
1
Cleared
0
Denied
Kaweco GmbH has 1 FDA 510(k) cleared medical devices. Based in Great Neck,, US.
Historical record: 1 cleared submissions from 1997 to 1997. Primary specialty: Obstetrics & Gynecology.
Browse the FDA 510(k) cleared devices submitted by Kaweco GmbH Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Kaweco GmbH
1 devices