Zeppelin Medizinlechnik GmbH is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Zeppelin Medizinlechnik GmbH - FDA 510(k) Cleared Devices
1
Total
1
Cleared
0
Denied
Zeppelin Medizinlechnik GmbH has 1 FDA 510(k) cleared medical devices. Based in Mchenry, US.
Historical record: 1 cleared submissions from 1977 to 1977. Primary specialty: Obstetrics & Gynecology.
Browse the FDA 510(k) cleared devices submitted by Zeppelin Medizinlechnik GmbH Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Zeppelin Medizinlechnik GmbH
1 devices